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United States · US · US:82046-884_52bb7505-a02a-2533-e063-6294a90a2520
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE BENZOYL PEROXIDE EFFACLAR BPO
UNIISPLATC D10AE01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerL�Oreal USA Products Inc
CountryUS (United States)
ATC codeD10AE01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1182046884011 TUBE in 1 CARTON (82046-884-01) / 20 mL in 1 TUBE
- ndc11820468840215 TUBE in 1 CARTON (82046-884-02) / 3 mL in 1 TUBE
- ndc1182046884031 TUBE in 1 CARTON (82046-884-03) / 40 mL in 1 TUBE
Annotations
UNII (FDA Substance ID)
W9WZN9A0GM
BENZOYL PEROXIDE
RxCUI 1418
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "W9WZN9A0GM",
"rxcui": "1418",
"inchikey": "OMPJBNCRMGITSC-UHFFFAOYSA-N",
"display_name": "BENZOYL PEROXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"851882ac-56f4-4bf6-b942-6efea10eec3e": {
"match": "brand_token",
"title": "LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE BENZOYL PEROXIDE EFFACLAR BPO (BENZOYL PEROXIDE) CREAM [L’OREAL USA PRODUCTS INC]",
"spl_version": "1",
"published_date": "2026-05-28"
}
},
"productid": "82046-884_52bb7505-a02a-2533-e063-6294a90a2520",
"productndc": "82046-884",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZOYL PEROXIDE",
"proprietary_name": "LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE BENZOYL PEROXIDE EFFACLAR BPO",
"active_ingred_unit": "mg/mL",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzoyl Peroxide",
"start_marketing_date": "20260522",
"active_numerator_strength": "55"
}Related drugs
Other records sharing ATC code D10AE01.
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