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United States · US · US:0316-0228_48342795-9bf1-4541-e063-6394a90a10be
PanOxyl
UNIISPLATC D10AE01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCrown Laboratories
CountryUS (United States)
ATC codeD10AE01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1103160228011 TUBE in 1 CARTON (0316-0228-01) / 28 g in 1 TUBE
- ndc11031602280385 g in 1 TUBE (0316-0228-03)
- ndc1103160228551 TUBE in 1 CARTON (0316-0228-55) / 156 g 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": {
"507150a0-9c20-4a2e-e063-6394a90ab9c7": {
"match": "brand_token",
"title": "PANOXYL ACNE CLEARING SPOT TREATMENT (BENZOYL PEROXIDE) GEL [CROWN LABORATORIES]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "0316-0228_48342795-9bf1-4541-e063-6394a90a10be",
"productndc": "0316-0228",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZOYL PEROXIDE",
"proprietary_name": "PanOxyl",
"active_ingred_unit": "mg/g",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "benzoyl peroxide",
"start_marketing_date": "20110325",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code D10AE01.
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