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United States Β· US Β· US:76159-004_0c5baaf8-ed44-5c24-e063-6394a90a9f3c
3LAB Aqua BB SPF 40 BROAD SPECTRUM 01
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
Manufacturer3LAB, Inc.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1176159004001 JAR in 1 CARTON (76159-004-00) / 28 mL in 1 JAR
Annotations
UNII (FDA Substance ID)
15FIX9V2JP
TITANIUM DIOXIDE
RxCUI 38323
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "15FIX9V2JP",
"rxcui": "38323",
"inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
"display_name": "TITANIUM DIOXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"2a2f5f9a-4e2f-4bbb-e063-6294a90ab99e": {
"match": "brand_token",
"title": "3LAB WW DAY SPF40 BROAD SPECTRUM (HOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE) CREAM [3LAB, INC]",
"spl_version": "1",
"published_date": "2024-12-30"
}
},
"productid": "76159-004_0c5baaf8-ed44-5c24-e063-6394a90a9f3c",
"productndc": "76159-004",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE",
"proprietary_name": "3LAB Aqua BB SPF 40 BROAD SPECTRUM 01",
"active_ingred_unit": "mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "TITANIUM DIOXIDE",
"start_marketing_date": "20131118",
"active_numerator_strength": "78.6"
}Access this data programmatically
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