non-tinted daily mineral shield
Generic: zinc oxide
Labeler: signature med spa mt llcDrug Facts
Product Profile
Brand Name
non-tinted daily mineral shield
Generic Name
zinc oxide
Labeler
signature med spa mt llc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 160 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
85896-226
Product ID
85896-226_4627c59e-c05d-f02d-e063-6294a90aba75
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2024-08-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85896226
Hyphenated Format
85896-226
Supplemental Identifiers
UPC
UNII
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
non-tinted daily mineral shield (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/g
Packaging
- 50 g in 1 BOTTLE, PUMP (85896-226-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4627c59e-c05d-f02d-e063-6294a90aba75", "openfda": {"upc": ["0385896226506"], "unii": ["SOI2LOH54Z"], "spl_set_id": ["3ab0298d-b2d0-591e-e063-6394a90a3177"], "manufacturer_name": ["SIGNATURE MED SPA MT LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE, PUMP (85896-226-50)", "package_ndc": "85896-226-50", "marketing_start_date": "20240802"}], "brand_name": "Non-Tinted Daily Mineral Shield", "product_id": "85896-226_4627c59e-c05d-f02d-e063-6294a90aba75", "dosage_form": "CREAM", "product_ndc": "85896-226", "generic_name": "Zinc Oxide", "labeler_name": "SIGNATURE MED SPA MT LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Non-Tinted Daily Mineral Shield", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "160 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240802", "listing_expiration_date": "20261231"}