mineral sunscreen
Generic: zinc oxide sunscreen
Labeler: bentley laboratories llcDrug Facts
Product Profile
Brand Name
mineral sunscreen
Generic Name
zinc oxide sunscreen
Labeler
bentley laboratories llc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 12.025 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
54111-183
Product ID
54111-183_8fbbcad3-e255-4f2a-9902-00f6316a253c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2020-12-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54111183
Hyphenated Format
54111-183
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
mineral sunscreen (source: ndc)
Generic Name
zinc oxide sunscreen (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.025 g/100mL
Packaging
- 1 TUBE in 1 CARTON (54111-183-01) / 42 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "8fbbcad3-e255-4f2a-9902-00f6316a253c", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["782a8641-7e6a-413b-a2ed-0efeb36c48a7"], "manufacturer_name": ["Bentley Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (54111-183-01) / 42 mL in 1 TUBE", "package_ndc": "54111-183-01", "marketing_start_date": "20201215"}], "brand_name": "Mineral Sunscreen", "product_id": "54111-183_8fbbcad3-e255-4f2a-9902-00f6316a253c", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "54111-183", "generic_name": "Zinc Oxide Sunscreen", "labeler_name": "Bentley Laboratories LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mineral Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "12.025 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201215", "listing_expiration_date": "20261231"}