scar gel spf 35

Generic: zinc oxide

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

Drug Facts

Product Profile

Brand Name scar gel spf 35
Generic Name zinc oxide
Labeler derma e
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

zinc oxide 117 mg/g

Manufacturer
derma e

Identifiers & Regulatory

Product NDC 54108-8111
Product ID 54108-8111_04ff8c03-d928-4bfd-88d5-3bf14b9da3c9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2020-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 541088111
Hyphenated Format 54108-8111

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 scar gel spf 35 (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 117 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 BOX (54108-8111-1) / 43 g in 1 TUBE
source: ndc

Packages (1)

54108-8111-1 1 TUBE in 1 BOX (54108-8111-1) / 43 g in 1 TUBE

Ingredients (1)

zinc oxide (117 mg/g)

Linked Drug Pages (1)

Scar Gel SPF 35 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "04ff8c03-d928-4bfd-88d5-3bf14b9da3c9", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["8cd263aa-a54b-4c55-b3e2-6f6763987d4a"], "manufacturer_name": ["derma e"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (54108-8111-1)  / 43 g in 1 TUBE", "package_ndc": "54108-8111-1", "marketing_start_date": "20200715"}], "brand_name": "Scar Gel SPF 35", "product_id": "54108-8111_04ff8c03-d928-4bfd-88d5-3bf14b9da3c9", "dosage_form": "CREAM", "product_ndc": "54108-8111", "generic_name": "Zinc Oxide", "labeler_name": "derma e", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Scar Gel", "brand_name_suffix": "SPF 35", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "117 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200715", "listing_expiration_date": "20261231"}