advanced light perfecting sunscreen
Generic: zinc oxide
Labeler: advanced dermatologyDrug Facts
Product Profile
Brand Name
advanced light perfecting sunscreen
Generic Name
zinc oxide
Labeler
advanced dermatology
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 160 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85351-208
Product ID
85351-208_4586c8f3-33e8-111f-e063-6394a90ad8dd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2021-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85351208
Hyphenated Format
85351-208
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
advanced light perfecting sunscreen (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/g
Packaging
- 50 g in 1 BOTTLE, PUMP (85351-208-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4586c8f3-33e8-111f-e063-6394a90ad8dd", "openfda": {"upc": ["0385351208504"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["32d781ca-7993-9875-e063-6294a90a5c26"], "manufacturer_name": ["ADVANCED DERMATOLOGY"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85351-208-50)", "package_ndc": "85351-208-50", "marketing_start_date": "20210901"}], "brand_name": "Advanced Light Perfecting Sunscreen", "product_id": "85351-208_4586c8f3-33e8-111f-e063-6394a90ad8dd", "dosage_form": "CREAM", "product_ndc": "85351-208", "generic_name": "Zinc Oxide", "labeler_name": "ADVANCED DERMATOLOGY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Light Perfecting Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}