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United States · US · US:71399-9478_4911da35-ce19-18af-e063-6394a90a5554
MEDPURA Benzoyl Peroxide
UNIISPLATC D10AE01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAkron Pharma Inc.
CountryUS (United States)
ATC codeD10AE01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1171399947851 TUBE in 1 CARTON (71399-9478-5) / 42.5 mL in 1 TUBE
- ndc1171399947861 TUBE in 1 CARTON (71399-9478-6) / 60 mL in 1 TUBE
- ndc1171399947891 TUBE in 1 CARTON (71399-9478-9) / 90 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": {
"b7d335d1-3022-4b28-913c-477152a7dad2": {
"match": "brand_token",
"title": "MEDPURA BENZOYL PEROXIDE AQUEOUS BASE, ACNE TREATMENT GEL (BENZOYL PEROXIDE) GEL [AKRON PHARMA INC.]",
"spl_version": "4",
"published_date": "2026-01-26"
}
},
"productid": "71399-9478_4911da35-ce19-18af-e063-6394a90a5554",
"productndc": "71399-9478",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZOYL PEROXIDE",
"proprietary_name": "MEDPURA Benzoyl Peroxide",
"active_ingred_unit": "mg/mL",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzoyl Peroxide",
"start_marketing_date": "20240913",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code D10AE01.
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