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United States · US · US:63621-354_43535ccc-3e06-c1e0-e063-6294a90a3acb
SunDrops 77
UNIISPLATC D08AJ01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSunburst Chemicals, Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1163621354404 BAG in 1 BOX (63621-354-40) / 1000 mL in 1 BAG
- ndc1163621354858 BAG in 1 BOX (63621-354-85) / 1000 mL in 1 BAG
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": {
"b0623424-939e-4b49-aa99-c1ef22cf0f2d": {
"match": "brand_token",
"title": "SUNDROPS 75 (ALCOHOL) GEL [SUNBURST CHEMICALS, INC.]",
"spl_version": "10",
"published_date": "2025-11-17"
}
},
"productid": "63621-354_43535ccc-3e06-c1e0-e063-6294a90a3acb",
"productndc": "63621-354",
"dosage_form": "SOAP",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZALKONIUM CHLORIDE",
"proprietary_name": "SunDrops 77",
"active_ingred_unit": "mg/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzalkonium Chloride",
"start_marketing_date": "20080505",
"active_numerator_strength": "1"
}Related drugs
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