tinted daily protection sunscreen
Generic: zinc oxide
Labeler: kemmi lee skin scienceDrug Facts
Product Profile
Brand Name
tinted daily protection sunscreen
Generic Name
zinc oxide
Labeler
kemmi lee skin science
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 160 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85711-208
Product ID
85711-208_461546fa-70f5-dad0-e063-6394a90a4675
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2024-04-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85711208
Hyphenated Format
85711-208
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
tinted daily protection 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 (85711-208-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "461546fa-70f5-dad0-e063-6394a90a4675", "openfda": {"upc": ["0860011751571"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["37ef5a05-54d2-a8e4-e063-6394a90a8e48"], "manufacturer_name": ["Kemmi Lee Skin Science"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85711-208-50)", "package_ndc": "85711-208-50", "marketing_start_date": "20240402"}], "brand_name": "Tinted Daily Protection Sunscreen", "product_id": "85711-208_461546fa-70f5-dad0-e063-6394a90a4675", "dosage_form": "CREAM", "product_ndc": "85711-208", "generic_name": "Zinc Oxide", "labeler_name": "Kemmi Lee Skin Science", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tinted Daily Protection Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240402", "listing_expiration_date": "20261231"}