Back to top

What this guide is and who it’s for?

This guide explains the science behind Colourstart® as a universal screening test for allergy to oxidative (permanent) hair colourants, with a focus on p‑phenylenediamine (PPD) and related dye ingredients.

It is written for hairdressers, salon owners, colour educators, manufacturers, insurers and other stakeholders who want a deeper, evidence‑based understanding rather than a marketing overview.

It brings together independent dermatology literature, real‑world Colourstart data, and public positions from UK regulators (including the Medicines and Healthcare products Regulatory Agency - MHRA) and industry bodies to show why a PPD‑based patch test can act as a practical universal screen for oxidative hair colour allergy.

Allergy to oxidative hair dyes: what we know

Permanent (oxidative) hair colourants are a recognised cause of allergic contact dermatitis (ACD). The main culprit is PPD, but closely related aromatic amines such as p‑toluenediamine (PTD), 2‑methoxymethyl‑PPD (ME‑PPD or ME+), p‑aminophenol (PAP) and m‑aminophenol (MAP) are also implicated.

Epidemiological data show that hair dye allergy is not rare. In the EDEN study, which included over 10,000 healthy adults (2,739 patch‑tested), the approximate prevalence of PPD contact allergy was 0.8%. Use of black henna tattoos, which often may contain illegally high concentrations of PPD, was strongly associated with later reactions to oxidative hair dye.

For hairdressers and their stakeholders, the key point is that while most clients will never experience a skin reaction, allergy to oxidative hair dye is common enough, and serious enough, that a structured approach to allergy screening makes professional sense.

Why PPD is used as a universal marker

Within the professional hairdressing supply chain, there is a persistent misconception that some oxidative hair colours are effectively “PPD‑free” in a way that removes allergy risk. In reality, most permanent oxidative dyes rely on a family of closely related para‑amines, of which PPD is the best‑known example.

Dermatologists worldwide include PPD (typically 1% in petrolatum) in the baseline patch test series as an index allergen for oxidative hair‑dye allergy diagnosis. In other words, PPD is widely used clinically as a marker allergen: if a patient reacts to PPD, this is taken as a strong indication of allergy to the broader group of para‑amine hair dyes. This is why PPD is so important in both clinical diagnosis and (salon) screening, even when a given hair colour product does not list “PPD” on the label but instead contains closely related substances.

Colourstart® as an MHRA‑licensed screening test

In 2018, Colourstart became the first and only MHRA‑licensed cutaneous patch test for screening allergy to PPD in consumers aged 16 years and over.

To obtain this licence, Colourstart had to demonstrate:

  • A high level of efficacy in identifying individuals allergic to PPD.
  • A very low chance of getting a “false positive” result.
  • Non-specialists were able to interpret any skin reaction seen.
  • An acceptable safety profile, including consideration of the risk of sensitisation.
  • Consistent manufacturing quality with a defined allergen dose in each patch.
  • Ongoing pharmacovigilance arrangements for monitoring and reporting adverse events.

For hairdressing professionals and their stakeholders, this means that Colourstart is not a self‑declared home‑made patch test; it is a regulated medical device that has been formally and independently assessed for performance, safety and quality.

See section 10.

Real‑world Colourstart data and what it shows

Since licensing, Colourstart has been used extensively by salons and consumers, and real‑world data have been presented twice at Congresses of the European Society of Contact Dermatitis (ESCD).

Two key datasets have been published in abstract form:

The positive rate of 0.7% is remarkably consistent across datasets and aligns well with European epidemiological estimates of PPD allergy prevalence (around 0.7–1%). Adverse events were rare, mild and non‑serious, and in the 2022 dataset, a pre‑screening questionnaire was used to identify individuals already highly likely to be allergic to hair dye; these consumers were advised not to apply the patch.

In practice, this suggests that Colourstart is detecting approximately the proportion of clients one would expect to be allergic to PPD based on independent studies, while the safety profile in large‑scale use has been very favourable.

Cross‑reactivity: PPD, PTD, ME‑PPD and related dyes

Allergic contact dermatitis to hair dyes does not exist in isolation for each separate ingredient. Many of the oxidative dye intermediates are structurally similar para‑amines, and the immune system can cross‑react between them.

Multiple studies have shown strong cross‑reactivity between PPD and other oxidative dye ingredients:

The positive rate of 0.7% is remarkably consistent across datasets and aligns well with European epidemiological estimates of PPD allergy prevalence (around 0.7–1%). Adverse events were rare, mild and non‑serious, and in the 2022 dataset, a pre‑screening questionnaire was used to identify individuals already highly likely to be allergic to hair dye; these consumers were advised not to apply the patch.

In practice, this suggests that Colourstart is detecting approximately the proportion of clients one would expect to be allergic to PPD based on independent studies, while the safety profile in large‑scale use has been very favourable.

ME‑PPD (ME+) and why PPD remains the screen

ME‑PPD (also known as ME+) has been introduced as a lower‑potency allergen alternative to PPD in some oxidative hair colour formulations.*

Human studies in PPD‑allergic individuals show that:

  • In open‑use tests with hair dyes containing 2% PPD or 2% ME‑PPD, about 48% of PPD‑allergic subjects also reacted to the ME‑PPD‑containing dye.

  • When ME‑PPD was patch‑tested at concentrations from 0.1% to 2.0%, cross‑elicitation rates rose to around 84% at higher concentrations.

These results indicate that although ME‑PPD is less potent than PPD, it is clearly cross‑reactive and should not be assumed to be safe for PPD‑allergic individuals. From a screening perspective, this supports the continued use of PPD as a relevant marker allergen, even for products formulated with ME‑PPD instead of PPD.

“PPD‑free” claims: ASA and CTPA positions

In recent years, “PPD‑free” claims have been used in marketing some oxidative hair colours. However, these products may still contain PPD‑related para‑amines, and regulators have taken a clear stance on this.

ASA ruling


In 2025, the UK Advertising Standards Authority (ASA) ruled on advertising for a hair‑colour range described as “PPD‑free” while containing PTD.

The ASA concluded that:

  • Despite the absence of PPD, the presence of PTD meant that PPD‑allergic individuals could still react.
  • Repeated “PPD‑free” claims and associated messaging were likely to give consumers the impression that those with PPD allergy were at little or no risk.
  • The advertisements were therefore misleading and irresponsible and should not be used again in that form.

CTPA guidance


The Cosmetic, Toiletry and Perfumery Association (CTPA), the UK trade association for cosmetics and personal‑care companies, has issued guidance on “PPD‑free” claims which states that:

  • Darker oxidative hair colours often require PPD‑related aromatic amines such as PTD or ME‑PPD.
  • Individuals allergic to PPD may also react to these related ingredients.
  • Products containing PPD or related para‑amines must be labelled with warnings such as “contains phenylenediamines (toluenediamines)”.
  • “PPD‑free” claims on products that still contain PPD‑related ingredients are regarded as misleading.
PROPERTYPPDPTDPAP/MAPME-PPD
CAS number106-50-395-70-5123-30-8337906-36-2 (base);
337906-37-3
(sulfate)
Chemical formulaC6H8N2C7H10N2C6H7N0C8H12N2O
Required pictograms
Signal wordDangerDangerWarningDanger

These public statements are consistent with the dermatology literature on cross‑reactivity and reinforce the need for honest, precise communication about allergenic para‑amines in hair colour products.

Manufacturer recommended 48‑hour Allergy Alert Tests (AATs)

Most oxidative hair colour manufacturers recommend a 48‑hour Allergy Alert Test (AAT) before use. Dermatology literature has discussed these tests critically, raising several concerns:

  • Standardisation
    Different brands recommend different test sites, allergen doses and exposure times. This lack of standardisation makes AATs difficult to compare or validate across products.
  • Allergen concentration
    Oxidative dye formulations used for AATs can contain PPD concentrations around 2%, which is higher than diagnostic patch‑test preparations used in specialist practice.
  • Frequency of exposure
    Consumers who colour their hair regularly may repeat the AAT several times per year, leading to repeated high‑dose exposure to potent sensitisers, potentially increasing the risk of becoming allergic.
  • Interpretation
    Accurate reading of allergic versus irritant reactions requires training. Untrained consumers can misinterpret redness or itching, resulting in either false reassurance (proceeding despite a reaction) or unnecessary avoidance.
  • Compliance
    In real‑world practice, AATs are not always carried out or documented consistently. Some clients skip them entirely; others may not follow instructions exactly.

These limitations mean that AATs are not equivalent to a standardised, regulated diagnostic tool, and they may themselves carry sensitisation risk when used repeatedly with high‑dose dye mixtures.

Why UK salons choose Colourstart over the Allergy Alert Test

UK salons chose to move away from relying on manufacturers’ Allergy Alert Testing system to 
adopt Colourstart in consideration of the following technical points:

  • The Allergy Alert Test design is not aligned with professional hair colour services. Inconsistency between on‑pack safety instructions and the variety of off-pack “protocols” proposed by some colour brands.
  • In contrast, the certainty of a standardised system across all professional colour brands means screening processes are the same irrespective of which oxidative colour range is being used. This allows businesses to establish a single approach to allergy screening that can be used to train staff and educate clients, keeping protocols clear, consistent and simple.

There is also a practical and professional issue around who performs allergy tests. With Colourstart, the client applies the test themselves and, by completing the associated questions, self‑certifies their suitability for colour. This keeps the allergy decision with the client and the licensed medicine, rather than relying on hairdressers to interpret skin reactions, and avoids the additional complexity of the Allergy Alert Test, where irritant reactions to components of the colour formulation 
can be difficult to distinguish from true allergy.

What this evidence means for professional colour practice

Taken together, the evidence leads to several clear conclusions:

  • PPD is widely recognised as the key marker allergen for oxidative hair‑dye allergy.
  • Cross‑reactivity between PPD and other oxidative dye intermediates (PTD, ME‑PPD, PAP, MAP) is well documented in the dermatology literature.
  • Real‑world Colourstart data from more than 58,000 uses show a positive rate (~0.7%) that is consistent with epidemiological estimates of PPD allergy, and adverse events have been extremely infrequent, mild and non‑serious.
  • ASA and CTPA documents emphasise that “PPD‑free” products containing PPD‑related ingredients may still pose a risk to PPD‑allergic individuals and that such claims can be misleading.
  • Dermatology papers raise questions about the standardisation, dose, frequency and interpretability of manufacturer 48‑hour AATs, particularly when repeated frequently.

For hairdressers and their stakeholders, this provides the context for using Colourstart as a PPD‑based universal screening test for individuals considering oxidative hair colouring. It offers a regulated, standardised way to screen for relevant allergy across the para‑amine dye family, supports professional duty of care, and can be integrated into salon protocols in place of, or alongside, traditional AATs.

References
  1. Thyssen JP et al. Contact Dermatitis. 2012;66:300–311.
  2. Orton D, Basketter DA. Contact Dermatitis. 2012;66:312–316.
  3. Basketter DA, English J. Cutan Ocul Toxicol. 2009;28:104–106.
  4. Søsted H et al. Contact Dermatitis. 2013;69:32–39.
  5. Schuttelaar ML et al. Contact Dermatitis. 2018;78:1–7.
  6. Pongpairoj et al. 2016.
  7. Diepgen TL et al. EDEN study, 2016.
  8. Basketter DA, Plunkett N, Andersen KE. ESCD poster, 2022.
  9. Basketter DA, Plunkett N, Andersen KE. ESCD poster, 2024.
  10. ASA ruling, Instituto Naturvita S.L. 2025.
  11. CTPA “PPD‑free?” FAQ, 2024.
  12. CTPA press release on ASA ruling, 2025.
  13. Pongpairoj, K, McFadden JP, Basketter DA. British Journal of Dermatology, 2016;174:957-958.