πΊπΈ
United States Β· US Β· US:82516-202_40a8a749-92b7-d0b4-e063-6294a90ae79f
Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTrue Botanicals
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1182516202021 BOTTLE, PUMP in 1 CARTON (82516-202-02) / 30 g in 1 BOTTLE, PUMP (82516-202-01)
Annotations
UNII (FDA Substance ID)
SOI2LOH54Z
ZINC OXIDE
RxCUI 11423
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SOI2LOH54Z",
"rxcui": "11423",
"inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
"display_name": "ZINC OXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"1cb7fbca-0874-ae53-e063-6294a90ab42a": {
"match": "brand_token",
"title": "SUNSCREEN FOR BABY SPF50PLUS (OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE) LOTION [GUANGZHOU SENMAI BIOTECHNOLOGY CO., LTD.]",
"spl_version": "7",
"published_date": "2026-04-03"
}
},
"productid": "82516-202_40a8a749-92b7-d0b4-e063-6294a90ae79f",
"productndc": "82516-202",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Sunscreen",
"active_ingred_unit": "g/100g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Everyday Skin Tint SPF 30",
"start_marketing_date": "20220616",
"active_numerator_strength": "18"
}Access this data programmatically
Query Sunscreen and 610,000+ other drug records through a single REST API β with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.