illuminating daily spf 40 lightly tinted
Generic: zinc oxide
Labeler: face 5, llcDrug Facts
Product Profile
Brand Name
illuminating daily spf 40 lightly tinted
Generic Name
zinc oxide
Labeler
face 5, llc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 160 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85302-208
Product ID
85302-208_4577d776-c5a8-f077-e063-6294a90a282e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2024-04-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85302208
Hyphenated Format
85302-208
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
illuminating daily spf 40 lightly tinted (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 (85302-208-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4577d776-c5a8-f077-e063-6294a90a282e", "openfda": {"upc": ["0385302208508"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["3001ef4f-4cbb-8931-e063-6394a90a5cef"], "manufacturer_name": ["Face 5, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85302-208-50)", "package_ndc": "85302-208-50", "marketing_start_date": "20240417"}], "brand_name": "Illuminating Daily SPF 40 Lightly Tinted", "product_id": "85302-208_4577d776-c5a8-f077-e063-6294a90a282e", "dosage_form": "CREAM", "product_ndc": "85302-208", "generic_name": "Zinc Oxide", "labeler_name": "Face 5, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Illuminating Daily SPF 40 Lightly Tinted", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240417", "listing_expiration_date": "20261231"}