dr lift spf 50 mineral sunscreen stick
Generic: zinc oxide
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
dr lift spf 50 mineral sunscreen stick
Generic Name
zinc oxide
Labeler
spa de soleil
Dosage Form
STICK
Routes
Active Ingredients
zinc oxide 3.75 g/15g
Manufacturer
Identifiers & Regulatory
Product NDC
68062-8314
Product ID
68062-8314_436fdf4f-11da-7c5b-e063-6294a90a8731
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-11-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680628314
Hyphenated Format
68062-8314
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
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
dr lift spf 50 mineral sunscreen stick (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3.75 g/15g
Packaging
- 15 g in 1 TUBE (68062-8314-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "436fdf4f-11da-7c5b-e063-6294a90a8731", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["436fdf4f-11db-7c5b-e063-6294a90a8731"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (68062-8314-1)", "package_ndc": "68062-8314-1", "marketing_start_date": "20251112"}], "brand_name": "Dr Lift SPF 50 Mineral Sunscreen Stick", "product_id": "68062-8314_436fdf4f-11da-7c5b-e063-6294a90a8731", "dosage_form": "STICK", "product_ndc": "68062-8314", "generic_name": "Zinc Oxide", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Lift SPF 50 Mineral Sunscreen Stick", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "3.75 g/15g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251112", "listing_expiration_date": "20261231"}