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United States · US · US:85131-013_b9f737e2-25dc-44cc-aa07-a5a77758473c
Durashield
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAdvanced Biomedical Incorporated
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc118513101300.33 mL in 1 BOTTLE (85131-013-00)
- ndc11851310130260 mL in 1 BOTTLE (85131-013-02)
- ndc118513101304118 mL in 1 BOTTLE (85131-013-04)
- ndc118513101308237 mL in 1 BOTTLE, PUMP (85131-013-08)
- ndc118513101312355 mL in 1 BOTTLE, PUMP (85131-013-12)
- ndc118513101316473 mL in 1 BOTTLE, PUMP (85131-013-16)
Annotations
UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F5UM2KM3W7",
"rxcui": "1379",
"inchikey": null,
"display_name": "BENZALKONIUM CHLORIDE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"b0723781-225a-46c6-907c-5c5c48f383b8": {
"match": "brand_token",
"title": "DURASHIELD (BENZALKONIUM CHLORIDE) LOTION [ADVANCED BIOMEDICAL INCORPORATED]",
"spl_version": "1",
"published_date": "2025-01-16"
}
},
"productid": "85131-013_b9f737e2-25dc-44cc-aa07-a5a77758473c",
"productndc": "85131-013",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "Durashield",
"active_ingred_unit": "mg/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "benzalkonium chloride",
"start_marketing_date": "20241218",
"active_numerator_strength": ".13"
}Related drugs
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