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United States · US · US:69396-071_3d0e3bad-3feb-651e-e063-6394a90aef17
Dual Action Cream
UNIISPLATC A01AB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTrifecta Pharmaceutical USA LLC
CountryUS (United States)
ATC codeA01AB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1169396071011 TUBE in 1 BOX (69396-071-01) / 28.4 g in 1 TUBE
- ndc1169396071222 TUBE in 1 BOX (69396-071-22) / 28.4 g in 1 TUBE
- ndc1169396071444 TUBE in 1 BOX (69396-071-44) / 28.4 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
057Y626693
NEOMYCIN SULFATE
RxCUI 7300
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "057Y626693",
"rxcui": "7300",
"inchikey": null,
"display_name": "NEOMYCIN SULFATE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"8d9a0c56-ef22-45a6-8b1d-d2b2f3247210": {
"match": "brand_token",
"title": "DUAL ACTION BACK PAIN RELIEVER (ACETAMINOPHEN, IBUPROFEN) TABLET, FILM COATED [MEIJER, INC.]",
"spl_version": "2",
"published_date": "2026-03-23"
}
},
"productid": "69396-071_3d0e3bad-3feb-651e-e063-6394a90aef17",
"productndc": "69396-071",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE",
"proprietary_name": "Dual Action Cream",
"active_ingred_unit": "mg/g; [USP'U]/g; mg/g",
"application_number": "M004",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL",
"start_marketing_date": "20210106",
"active_numerator_strength": "3.5; 10000; 10"
}Related drugs
Other records sharing ATC code A01AB.
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