NEUTROGENA SUNBLOCK SPF 30 (produit inactif : annulé après commercialisation : 10 août 1999)
Nonprescription drug in Canada (DIN); Cancelled after marketing: 10 August 1999
A nonprescription drug in Canada may have a cancelled status. Their presence does not demonstrate current sales. The DIN is the drug identification number printed on the packaging. The analysis indicates what the annexes to Regulation (EC) No 1223/2009 would require if this product were sold as a cosmetic in France. It does not assess its Canadian authorisation and does not constitute authorisation for sale in France. Only active ingredients are published in these extracts; the full formula and other conditions of use remain to be checked. No strength is estimated.
Drug Product Database, Canadian non-prescription drugs with cosmetic uses, retrieved 27 October 2026.
Contains information licensed under the Open Government Licence – Canada (Health Canada, DPD)
- DIN
- 02229370
- Trade name
- NEUTROGENA SUNBLOCK SPF 30
- Company
- PROFESSIONAL PHARMACEUTICAL CORP. / CORP. PHARMACEUTIQUE PROFESSIONNELLE
- Current status
- Cancelled after marketing: 10 August 1999
- Product update in the source
- 22 March 2025
- Form
- Crème
- Routes
- Topique
- ATC classes
- D02BA30 : French label not published
Status history
- Marketed: 15 July 1997
- Cancelled after marketing: 10 August 1999; current status
Published active ingredients and strengths
| Published active ingredient | Published strength | Percentage conversion |
|---|---|---|
| OCTISALATE | 5 %; published reference: % | 5 % (unspecified basis) |
| MERADIMATE | 5 %; published reference: % | 5 % (unspecified basis) |
| OCTOCRYLENE | 8 %; published reference: % | 8 % (unspecified basis) |
| OCTINOXATE | 7.5 %; published reference: % | 7,5 % (unspecified basis) |
Mass/volume percentages are not treated as mass/mass percentages. A strength expressed as base is not converted to the strength of the salt or compound.
Cosmetic analysis in the European Union
- OCTISALATE : Filtre UV autorisé sous les conditions de l’annexe VI du règlement (CE) 1223/2009.
- Annexe VI, entrée 20 : 5 % ; comparaison de teneur non établie sans estimation.
- MERADIMATE : Cet ingrédient ne figure pas dans l’annexe VI et ne pourrait pas être utilisé comme filtre UV dans un cosmétique. Sa fonction UV dans ce produit n’est pas établie par l’extrait.
- OCTOCRYLENE : Filtre UV autorisé sous les conditions de l’annexe VI du règlement (CE) 1223/2009.
- Annexe VI, entrée 10 : a) 9 % b) 10 % Footnote (*3): Benzophenone as an impurity and/or degradation product of Octocrylene shall be kept at trace level. ; seulement pour : a) Propellant spray products b) Other products ; comparaison de teneur non établie sans estimation.
- OCTINOXATE : Filtre UV autorisé sous les conditions de l’annexe VI du règlement (CE) 1223/2009.
- Annexe VI, entrée 12 : 10 % ; comparaison de teneur non établie sans estimation.
3 ingredients allowed under conditions (maximum concentration, product types): some active ingredient concentrations are printed; the other conditions and the product's classification in the European Union remain to be checked. 4 names recognised out of 4.
ETHYLHEXYL SALICYLATE, MENTHYL ANTHRANILATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE
Who it concerns
For each group, the ingredients of the list that an official classification or rule mentions. Open an ingredient's page to read what the text says. A group with no name does not mean the ingredients were judged to have no effect for it.
No official text covers the recognised ingredients for: pregnancy and breastfeeding, babies and children, skin, eyes and allergies, environment, read on the label.
For a question about your own situation (pregnancy, child, allergy), show this list to your doctor, midwife or pharmacist: we cannot say whether this product suits you.
Selling elsewhere
Ingredients of this list that are prohibited, prohibited in some cases or subject to conditions in the other countries whose rules we record (nothing changes for sale in France). Absence is not approval: several countries only allow the preservatives, UV filters and colorants on their lists, and the function of an ingredient in the product is not known. What is covered for each country.
| Country | Prohibited | Prohibited in some cases | Subject to conditions |
|---|---|---|---|
| United Kingdom | - | - | ETHYLHEXYL SALICYLATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE |
| South Korea | - | - | ETHYLHEXYL SALICYLATE, MENTHYL ANTHRANILATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE |
| Australia | - | - | MENTHYL ANTHRANILATE, OCTOCRYLENE |
| ASEAN | - | - | ETHYLHEXYL SALICYLATE, MENTHYL ANTHRANILATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE |
| Taiwan | - | - | ETHYLHEXYL SALICYLATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE |
| Brazil | - | - | ETHYLHEXYL SALICYLATE, MENTHYL ANTHRANILATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE |
No prohibition or condition found in the recorded lists for: United States (federal), Washington State, California, Canada, Japan, China.
Ingredient by ingredient
The line under each name gives its rule in the European Union (legend below). Click a name for its page.
Hover over or tap a badge for its meaning.
Classified hazard (cancer, DNA, reproduction): Carcinogenic, mutagenic or toxic for reproduction under the CLPEU regulation that classifies chemicals by their hazards (EC No 1272/2008). Regulation, or identified endocrine disruptor. Irritation, allergy and environment: see “Who it concerns”.
| On the label | Glossary name | Rule in the European Union | Classified hazard (cancer, DNA, reproduction) |
|---|---|---|---|
| ETHYLHEXYL SALICYLATE | ETHYLHEXYL SALICYLATE | UV filter allowed under conditions (Annex VI) Annex VI, entry 20: maximum concentration: 5% | none |
| MENTHYL ANTHRANILATE | MENTHYL ANTHRANILATE | No specific rule in the Cosmetics Regulation | none |
| OCTOCRYLENE | OCTOCRYLENE | UV filter allowed under conditions (Annex VI) Annex VI, entry 10: products: a) Propellant spray products b) Other products; maximum concentration: a) 9% b) 10% Footnote (*3): Benzophenone as an impurity and/or degradation product of Octocrylene shall be kept at trace level. | none |
| ETHYLHEXYL METHOXYCINNAMATE | ETHYLHEXYL METHOXYCINNAMATE | UV filter allowed under conditions (Annex VI) Annex VI, entry 12: maximum concentration: 10% | none |
Official Drug Product Database record.
Contient des informations visées par la Licence du gouvernement ouvert – Canada (Santé Canada, BDPP).