Menthol and 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: Menthol and Zinc Oxide
Generic name: MENTHOL AND ZINC OXIDE
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: d0e43651-4215-465b-9ace-1bc23126b109
SPL ID: 2758f00d-dee3-2463-e063-6294a90a53c2
Version: 13
Effective date: 2024-11-20
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:32

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Menthol and Zinc Oxide	openfda.brand_name
generic name		MENTHOL AND ZINC OXIDE	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-234-03	openfda.package_ndc
ndc	package	67777-234-04	openfda.package_ndc
ndc	package	67777-234-02	openfda.package_ndc
ndc	package	67777-234-01	openfda.package_ndc
ndc	product	67777-234	openfda.product_ndc
ndc11	package	67777023403	derived:openfda.package_ndc
ndc11	package	67777023401	derived:openfda.package_ndc
ndc11	package	67777023404	derived:openfda.package_ndc
ndc11	package	67777023402	derived:openfda.package_ndc
rxcui		2123045	openfda.rxcui
spl id		2758f00d-dee3-2463-e063-6294a90a53c2	id
spl set id		d0e43651-4215-465b-9ace-1bc23126b109	set_id
unii		L7T10EIP3A	openfda.unii
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 Do not use section • On deep or puncture wounds 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.