dermatone spf 50 sunscreen stick
Generic: zinc oxide
Labeler: dermatoneDrug Facts
Product Profile
Brand Name
dermatone spf 50 sunscreen stick
Generic Name
zinc oxide
Labeler
dermatone
Dosage Form
STICK
Routes
Active Ingredients
zinc oxide 200 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
54414-108
Product ID
54414-108_461aa4d0-ff43-eafa-e063-6394a90ac22a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
352
Listing Expiration
2026-12-31
Marketing Start
2025-12-16
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54414108
Hyphenated Format
54414-108
Supplemental Identifiers
UPC
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
dermatone spf 50 sunscreen stick (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
352 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/g
Packaging
- 14 g in 1 CONTAINER (54414-108-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "461aa4d0-ff43-eafa-e063-6394a90ac22a", "openfda": {"upc": ["0020908051003"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["360ccf8c-47fb-4b01-ae44-527d714bfeed"], "manufacturer_name": ["Dermatone"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 g in 1 CONTAINER (54414-108-01)", "package_ndc": "54414-108-01", "marketing_start_date": "20251216"}], "brand_name": "Dermatone SPF 50 Sunscreen Stick", "product_id": "54414-108_461aa4d0-ff43-eafa-e063-6394a90ac22a", "dosage_form": "STICK", "product_ndc": "54414-108", "generic_name": "Zinc Oxide", "labeler_name": "Dermatone", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dermatone SPF 50 Sunscreen Stick", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "352", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251216", "listing_expiration_date": "20261231"}