zinc oxide
Generic: zinc oxide ointment
Labeler: derma sciences canada inc.Drug Facts
Product Profile
Brand Name
zinc oxide
Generic Name
zinc oxide ointment
Labeler
derma sciences canada inc.
Dosage Form
OINTMENT
Routes
Active Ingredients
zinc oxide .2 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
64772-201
Product ID
64772-201_37eff762-1eaa-ec66-e063-6394a90a3d10
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2014-11-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64772201
Hyphenated Format
64772-201
Supplemental Identifiers
RxCUI
UPC
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
zinc oxide (source: ndc)
Generic Name
zinc oxide ointment (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 g/g
Packaging
- 453.6 g in 1 JAR (64772-201-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "37eff762-1eaa-ec66-e063-6394a90a3d10", "openfda": {"upc": ["0361554002224"], "unii": ["SOI2LOH54Z"], "rxcui": ["198911"], "spl_set_id": ["37eff762-1ea9-ec66-e063-6394a90a3d10"], "manufacturer_name": ["Derma Sciences Canada Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "453.6 g in 1 JAR (64772-201-01)", "package_ndc": "64772-201-01", "marketing_start_date": "20141103"}], "brand_name": "Zinc Oxide", "product_id": "64772-201_37eff762-1eaa-ec66-e063-6394a90a3d10", "dosage_form": "OINTMENT", "product_ndc": "64772-201", "generic_name": "Zinc Oxide Ointment", "labeler_name": "Derma Sciences Canada Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zinc Oxide", "active_ingredients": [{"name": "ZINC OXIDE", "strength": ".2 g/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141103", "listing_expiration_date": "20261231"}