derma e sun protection mineral spf 30

Generic: zinc oxide

Labeler: derma e
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name derma e sun protection mineral spf 30
Generic Name zinc oxide
Labeler derma e
Dosage Form POWDER
Routes
TOPICAL
Active Ingredients

zinc oxide 241 mg/g

Manufacturer
derma e

Identifiers & Regulatory

Product NDC 54108-1486
Product ID 54108-1486_6b91329e-7dde-4226-8521-7f3c417a8b9e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-02-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 541081486
Hyphenated Format 54108-1486

Supplemental Identifiers

UNII
SOI2LOH54Z

Packaging Origin

Original Packager
true

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 derma e sun protection mineral spf 30 (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 241 mg/g
source: ndc
Packaging
  • 1 BOTTLE, WITH APPLICATOR in 1 BOX (54108-1486-1) / 5 g in 1 BOTTLE, WITH APPLICATOR
source: ndc

Packages (1)

Ingredients (1)

zinc oxide (241 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "6b91329e-7dde-4226-8521-7f3c417a8b9e", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["bb8e3df2-23e8-4ad0-a662-ff02d156e7b1"], "manufacturer_name": ["derma e"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 BOX (54108-1486-1)  / 5 g in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "54108-1486-1", "marketing_start_date": "20240226"}], "brand_name": "Derma E Sun Protection Mineral SPF 30", "product_id": "54108-1486_6b91329e-7dde-4226-8521-7f3c417a8b9e", "dosage_form": "POWDER", "product_ndc": "54108-1486", "generic_name": "Zinc oxide", "labeler_name": "derma e", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Derma E Sun Protection Mineral", "brand_name_suffix": "SPF 30", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "241 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240226", "listing_expiration_date": "20261231"}