Zinc Oxide

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Zinc Oxide
Generic name: ZINC OXIDE OINTMENT
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 11d79dd6-35f7-4399-e063-6294a90ac7dd
SPL ID: 4f5b6507-0292-edc3-e063-6294a90a3c79
Version: 2
Effective date: 2026-04-13
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:33

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Zinc Oxide	openfda.brand_name
generic name		ZINC OXIDE OINTMENT	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-223-01	openfda.package_ndc
ndc	package	67777-223-03	openfda.package_ndc
ndc	package	67777-223-02	openfda.package_ndc
ndc	package	67777-223-05	openfda.package_ndc
ndc	package	67777-223-06	openfda.package_ndc
ndc	package	67777-223-11	openfda.package_ndc
ndc	package	67777-223-13	openfda.package_ndc
ndc	package	67777-223-04	openfda.package_ndc
ndc	product	67777-223	openfda.product_ndc
ndc11	package	67777022313	derived:openfda.package_ndc
ndc11	package	67777022304	derived:openfda.package_ndc
ndc11	package	67777022305	derived:openfda.package_ndc
ndc11	package	67777022302	derived:openfda.package_ndc
ndc11	package	67777022303	derived:openfda.package_ndc
ndc11	package	67777022301	derived:openfda.package_ndc
ndc11	package	67777022306	derived:openfda.package_ndc
ndc11	package	67777022311	derived:openfda.package_ndc
rxcui		198911	openfda.rxcui
spl id		4f5b6507-0292-edc3-e063-6294a90a3c79	id
spl set id		11d79dd6-35f7-4399-e063-6294a90ac7dd	set_id
unii		SOI2LOH54Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For External Use Only When using this product • Avoid contact with eyes. Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.