Pharmacy Choice

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: Pharmacy Choice
Generic name: MENTHOL, ZINC OXIDE
Manufacturer: PHARMACY CHOICE INC
Product type: HUMAN OTC DRUG
SPL set ID: 5031fc05-e1c7-40b1-e063-6394a90aa12c
SPL ID: 5031fc05-e1c8-40b1-e063-6394a90aa12c
Version: 1
Effective date: 2026-04-24
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:36:13

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Pharmacy Choice	openfda.brand_name
generic name		MENTHOL, ZINC OXIDE	openfda.generic_name
manufacturer name		PHARMACY CHOICE INC	openfda.manufacturer_name
ndc	package	87228-3010-1	openfda.package_ndc
ndc	product	87228-3010	openfda.product_ndc
ndc11	package	87228301001	derived:openfda.package_ndc
rxcui		2123045	openfda.rxcui
spl id		5031fc05-e1c8-40b1-e063-6394a90aa12c	id
spl set id		5031fc05-e1c7-40b1-e063-6394a90aa12c	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 Not for deep or puncture wounds Avoid contact with eyes In case of accidental ingestion, contact a physician or posion control immediately If condition worsens or does not improve in 7 days, consult a doctor Do not put this product into the rectum by using fingers or any machanical device or applicator Children under 12 years of age: consult a doctor

Reported adverse events (FAERS/openFDA)#

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