daily skin protection sunscreen tinted
Generic: zinc oxide
Labeler: skinplusbyoroyo llcDrug Facts
Product Profile
Brand Name
daily skin protection sunscreen tinted
Generic Name
zinc oxide
Labeler
skinplusbyoroyo llc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 160 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85479-208
Product ID
85479-208_46019888-02ad-317e-e063-6394a90a5f35
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-04-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85479208
Hyphenated Format
85479-208
Supplemental Identifiers
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
daily skin protection sunscreen tinted (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/g
Packaging
- 1.5 g in 1 PACKET (85479-208-15)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "46019888-02ad-317e-e063-6394a90a5f35", "openfda": {"upc": ["0385479208158"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["35a9ecd7-b416-0aab-e063-6294a90a323d"], "manufacturer_name": ["SKINPLUSBYOROYO LLC"]}, "finished": true, "packaging": [{"sample": true, "description": "1.5 g in 1 PACKET (85479-208-15)", "package_ndc": "85479-208-15", "marketing_start_date": "20250421"}], "brand_name": "Daily Skin Protection Sunscreen Tinted", "product_id": "85479-208_46019888-02ad-317e-e063-6394a90a5f35", "dosage_form": "CREAM", "product_ndc": "85479-208", "generic_name": "Zinc Oxide", "labeler_name": "SKINPLUSBYOROYO LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daily Skin Protection Sunscreen Tinted", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250421", "listing_expiration_date": "20261231"}