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United States · US · US:63621-356_435330fc-c021-151b-e063-6394a90a229b
SunDrops 75
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSunburst Chemicals, Inc.
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc1163621356143785 mL in 1 BOTTLE, PLASTIC (63621-356-14)
- ndc1163621356208 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAG
- ndc11636213562512 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMP
- ndc1163621356404 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAG
- ndc116362135650473.2 mL in 1 BOTTLE, PUMP (63621-356-50)
Annotations
UNII (FDA Substance ID)
3K9958V90M
ALCOHOL
RxCUI 448
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "3K9958V90M",
"rxcui": "448",
"inchikey": "LFQSCWFLJHTTHZ-UHFFFAOYSA-N",
"display_name": "ALCOHOL",
"substance_type": "chemical",
"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": "63621-356_435330fc-c021-151b-e063-6394a90a229b",
"productndc": "63621-356",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "SunDrops 75",
"active_ingred_unit": "mL/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Alcohol",
"start_marketing_date": "20091014",
"active_numerator_strength": ".6"
}Related drugs
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