ultra zinc mineral non tinted

Generic: zinc oxide

Labeler: skin therapy studio llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra zinc mineral non tinted
Generic Name zinc oxide
Labeler skin therapy studio llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

zinc oxide 200 mg/g

Manufacturer
Skin Therapy Studio LLC

Identifiers & Regulatory

Product NDC 85357-205
Product ID 85357-205_460034b5-db8a-53e5-e063-6394a90a1ca6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-03-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85357205
Hyphenated Format 85357-205

Supplemental Identifiers

UNII
SOI2LOH54Z

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 ultra zinc mineral non tinted (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/g
source: ndc
Packaging
  • 1.5 g in 1 PACKET (85357-205-15)
source: ndc

Packages (1)

Ingredients (1)

zinc oxide (200 mg/g)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "460034b5-db8a-53e5-e063-6394a90a1ca6", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["35806102-6919-116f-e063-6294a90ad922"], "manufacturer_name": ["Skin Therapy Studio LLC"]}, "finished": true, "packaging": [{"sample": true, "description": "1.5 g in 1 PACKET (85357-205-15)", "package_ndc": "85357-205-15", "marketing_start_date": "20240313"}], "brand_name": "Ultra Zinc Mineral Non Tinted", "product_id": "85357-205_460034b5-db8a-53e5-e063-6394a90a1ca6", "dosage_form": "CREAM", "product_ndc": "85357-205", "generic_name": "Zinc Oxide", "labeler_name": "Skin Therapy Studio LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Zinc Mineral Non Tinted", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240313", "listing_expiration_date": "20261231"}