zinc oxide

Generic: zinc oxide ointment

Labeler: dynarex corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name zinc oxide
Generic Name zinc oxide ointment
Labeler dynarex corporation
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

zinc oxide 200 mg/g

Manufacturer
Dynarex Corporation

Identifiers & Regulatory

Product NDC 67777-223
Product ID 67777-223_11d79dd6-35f8-4399-e063-6294a90ac7dd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2024-02-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67777223
Hyphenated Format 67777-223

Supplemental Identifiers

RxCUI
198911
UPC
0616784119113 0616784119014 0616784119212
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 zinc oxide (source: ndc)
Generic Name zinc oxide ointment (source: ndc)
Application Number M016 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/g
source: ndc
Packaging
  • 72 BOX in 1 CASE (67777-223-02) / 1 TUBE in 1 BOX (67777-223-11) / 28.4 g in 1 TUBE (67777-223-01)
  • 72 BOX in 1 CASE (67777-223-04) / 1 TUBE in 1 BOX (67777-223-13) / 56.7 g in 1 TUBE (67777-223-03)
  • 12 JAR in 1 CASE (67777-223-06) / 425 g in 1 JAR (67777-223-05)
source: ndc

Packages (3)

67777-223-02 72 BOX in 1 CASE (67777-223-02) / 1 TUBE in 1 BOX (67777-223-11) / 28.4 g in 1 TUBE (67777-223-01) 67777-223-04 72 BOX in 1 CASE (67777-223-04) / 1 TUBE in 1 BOX (67777-223-13) / 56.7 g in 1 TUBE (67777-223-03) 67777-223-06 12 JAR in 1 CASE (67777-223-06) / 425 g in 1 JAR (67777-223-05)

Ingredients (1)

zinc oxide (200 mg/g)

Linked Drug Pages (1)

Zinc Oxide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "11d79dd6-35f8-4399-e063-6294a90ac7dd", "openfda": {"upc": ["0616784119113", "0616784119014", "0616784119212"], "unii": ["SOI2LOH54Z"], "rxcui": ["198911"], "spl_set_id": ["11d79dd6-35f7-4399-e063-6294a90ac7dd"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 BOX in 1 CASE (67777-223-02)  / 1 TUBE in 1 BOX (67777-223-11)  / 28.4 g in 1 TUBE (67777-223-01)", "package_ndc": "67777-223-02", "marketing_start_date": "20240229"}, {"sample": false, "description": "72 BOX in 1 CASE (67777-223-04)  / 1 TUBE in 1 BOX (67777-223-13)  / 56.7 g in 1 TUBE (67777-223-03)", "package_ndc": "67777-223-04", "marketing_start_date": "20240229"}, {"sample": false, "description": "12 JAR in 1 CASE (67777-223-06)  / 425 g in 1 JAR (67777-223-05)", "package_ndc": "67777-223-06", "marketing_start_date": "20240229"}], "brand_name": "Zinc Oxide", "product_id": "67777-223_11d79dd6-35f8-4399-e063-6294a90ac7dd", "dosage_form": "OINTMENT", "product_ndc": "67777-223", "generic_name": "Zinc Oxide Ointment", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zinc Oxide", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240229", "listing_expiration_date": "20261231"}