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United States · US · US:85339-212_45b3a9bc-1124-4545-e063-6394a90a5a58
Lip Protection
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeton Dermatology Holdings, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1185339212451 CYLINDER in 1 CARTON (85339-212-45) / 4.5 g in 1 CYLINDER
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": {
"a3e5819a-5132-9760-e053-2a95a90a058b": {
"match": "brand_token",
"title": "LIP SCREEN BROAD SPECTRUM SPF 40 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LIQUID [SUPERGOOP, LLC]",
"spl_version": "7",
"published_date": "2026-01-12"
}
},
"productid": "85339-212_45b3a9bc-1124-4545-e063-6394a90a5a58",
"productndc": "85339-212",
"dosage_form": "STICK",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
"proprietary_name": "Lip Protection",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Titanium Dioxide, Zinc Oxide",
"start_marketing_date": "20231027",
"active_numerator_strength": "40; 55"
}Access this data programmatically
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