🇺🇸
United States · US · US:68599-5201_2731720b-d98c-9dbf-e063-6394a90a054a
Premium Hand Sanitizer
UNIISPLATC D08AX08
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMCKESSON MEDICAL-SURGICAL INC.
CountryUS (United States)
ATC codeD08AX08
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc116859952011118 g in 1 PACKAGE (68599-5201-1)
- ndc116859952012237 g in 1 PACKAGE (68599-5201-2)
- ndc116859952013532 g in 1 PACKAGE (68599-5201-3)
- ndc1168599520141000 g in 1 PACKAGE (68599-5201-4)
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": {
"4a7e868d-6310-6ee4-e063-6394a90aebce": {
"match": "brand_token",
"title": "PREMIUM BEAUTY BALM BROAD SPECTRUM SPF 30 (OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AND ZINC OXIDE) LOTION [HAVE & BE CO., LTD.]",
"spl_version": "2",
"published_date": "2026-05-11"
}
},
"productid": "68599-5201_2731720b-d98c-9dbf-e063-6394a90a054a",
"productndc": "68599-5201",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALCOHOL",
"proprietary_name": "Premium Hand Sanitizer",
"active_ingred_unit": "g/100g",
"application_number": "M003",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "ethanol",
"start_marketing_date": "20150109",
"active_numerator_strength": "70"
}Related drugs
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