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United States · US · US:72476-947_4a2cca74-18c4-c52a-e063-6394a90a31bc
Sunscreen for Babies SPF 50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRetail Business Services, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117247694734236 mL in 1 BOTTLE, PLASTIC (72476-947-34)
Annotations
UNII (FDA Substance ID)
G63QQF2NOX
AVOBENZONE
RxCUI 45045
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G63QQF2NOX",
"rxcui": "45045",
"inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
"display_name": "AVOBENZONE",
"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": "72476-947_4a2cca74-18c4-c52a-e063-6394a90a31bc",
"productndc": "72476-947",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE",
"proprietary_name": "Sunscreen for Babies SPF 50",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Avobenzone, Homosalate, Octisalate",
"start_marketing_date": "20231219",
"active_numerator_strength": "30; 120; 50"
}Access this data programmatically
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