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United States · US · US:49404-157_51291c13-9634-7263-e063-6294a90a4d39
PREMIUM BEAUTY BALM BROAD SPECTRUM SPF 30
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHave & Be Co., Ltd.
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1149404157011 TUBE in 1 CARTON (49404-157-01) / 40 mL in 1 TUBE
- ndc1149404157991 mL in 1 PACKET (49404-157-99)
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"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": "49404-157_51291c13-9634-7263-e063-6294a90a4d39",
"productndc": "49404-157",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE",
"proprietary_name": "PREMIUM BEAUTY BALM BROAD SPECTRUM SPF 30",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE",
"start_marketing_date": "20260209",
"active_numerator_strength": "68; 45; 48; 50"
}Related drugs
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