🇺🇸
United States · US · US:58980-913_119ef16e-c873-41df-9e98-4ccade286a85
Peviderm Pramoxine Hydrocholride 1%
UNIISPLATC D04AB07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerStratus Pharmaceuticals Inc
CountryUS (United States)
ATC codeD04AB07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1158980913801 BOTTLE in 1 BOX (58980-913-80) / 222 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
88AYB867L5
PRAMOXINE HYDROCHLORIDE
RxCUI 57555
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "88AYB867L5",
"rxcui": "57555",
"inchikey": "SYCBXBCPLUFJID-UHFFFAOYSA-N",
"display_name": "PRAMOXINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"680b40fa-1922-443a-a4b0-7c3f6a2b847d": {
"match": "brand_token",
"title": "PEVIDERM PRAMOXINE HYDROCHOLRIDE 1% (PRAMOXINE HYDROCHLORIDE) LOTION [STRATUS PHARMACEUTICALS INC]",
"spl_version": "2",
"published_date": "2024-11-11"
}
},
"productid": "58980-913_119ef16e-c873-41df-9e98-4ccade286a85",
"productndc": "58980-913",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PRAMOXINE HYDROCHLORIDE",
"proprietary_name": "Peviderm Pramoxine Hydrocholride 1%",
"active_ingred_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Pramoxine Hydrochloride",
"start_marketing_date": "20241101",
"active_numerator_strength": "1"
}Related drugs
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