Therapeutic Menthol

Manufacturer: Product Quest Mfg
Effective date: 2018-08-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:31

Label at a glance#

ProductTherapeutic Menthol

Active ingredientMenthol

Label structure6 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose
Menthol 2%...........................................External Analgesic

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of minor aches and pains
of muscles and joints associated with simple backache,
arthritis, strains, bruises and sprains

WARNINGS SECTION

Warnings
For external use only
When using this product • avoid
contact with eyes • do not bandage tightly • do not apply to
wounds or damaged skin • do not use with a heating pad
Stop use and ask doctor if condition worsens or if
symptoms persist for 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 right away

DOSAGE & ADMINISTRATION SECTION

Directions
• for adults & children 2 years of age and older
• cleanse and dry skin
• apply to affected area not more than 3 to 4 times daily
• children under 2 years of age, consult a doctor

INACTIVE INGREDIENT SECTION

Inactive ingredients

Ammonium Hydroxide,
Carbomer, Cupric Sulfate, FD&C Blue No. 1, Isopropyl
Alcohol, Magnesium Sulfate, Purified Water, Sodium
Hydroxide, Thymol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
311502	menthol 2 % Topical Gel	PSN	1
311502	menthol 0.02 MG/MG Topical Gel	SCD	1
311502	menthol 2 % Topical Gel	SY	1
311502	menthol 2 % topical stick	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0727510007397	GTIN-13: 0727510007397 EAN-13: 0727510007397 GTIN-12: 727510007397 UPC-A: 727510007397 GTIN storage (14 digits): 00727510007397	label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64048-5117-7	2020-01-31	C162847	48780-1	9d75b9d0-62d7-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64048-5117-7	Therapeutic Menthol	227 g in 1 JAR	GEL	227		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64048-5117	THERAPEUTIC MENTHOL (MENTHOL 2.00%) GEL [PRODUCT QUEST MFG]	1	Legacy NDC, 1 package rows	20180807_bf5a1281-7044-4c0e-97f5-331886ae92e8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

Therapeutic Menthol
Menthol 2.00%
Menthol
AMMONIA
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)
Cupric Sulfate
FD&C BLUE NO. 1
Isopropyl Alcohol
MAGNESIUM SULFATE, UNSPECIFIED FORM
WATER
Sodium Hydroxide
Thymol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64048-5117	64048-5117-7

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Menthol	L7T10EIP3A	ACTIB
AMMONIA	5138Q19F1X	IACT
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)	Z135WT9208	IACT
Cupric Sulfate	LRX7AJ16DT	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
Isopropyl Alcohol	ND2M416302	IACT
MAGNESIUM SULFATE, UNSPECIFIED FORM	DE08037SAB	IACT
WATER	059QF0KO0R	IACT
Sodium Hydroxide	55X04QC32I	IACT
Thymol	3J50XA376E	IACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
84801e26-b6e9-47d8-928c-05302ef4ce5f			bf5a1281-7044-4c0e-97f5-331886ae92e8	2018-08-07	Warnings	Exact identifier spl id: 84801e26-b6e9-47d8-928c-05302ef4ce5f spl set id: bf5a1281-7044-4c0e-97f5-331886ae92e8

Reported adverse events (FAERS/openFDA)#

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