PHARMACYS PRESCRIPTION

Manufacturer: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO LTD
Effective date: 2014-07-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 01:35:01

Label at a glance#

ProductPHARMACYS PRESCRIPTION

Active ingredientMENTHOL

Label structure8 sections

Dosage and administration

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age, do not use, consult a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 1%

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age, do not use, consult a doctor.

PURPOSE

INDICATIONS & USAGE SECTION

Pain relieving gel

PURPOSE

OTC - PURPOSE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes, do not bandage tightly, do not apply to wounds or damaged skin, do not use with heating pads or other heating devices.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

carbomer, isopropyl alcohol, nonylphenylpolyoxyethylene ether, camphor, kathon CG, FD&C blue no.1, triethanolamine, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76176-017-08	2020-01-31	C162847	48780-1	9d75b9d0-0d72-f424-e053-dadaa90a57ce	223814fd-2a5b-4d3f-a65c-aeec5c6d2eb4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	2
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

PHARMACYS PRESCRIPTION
ANALGESIC
MENTHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76176-017	76176-017-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

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
b1b6f9cd-d97f-4788-a761-8bc0a9e2ccf6			223814fd-2a5b-4d3f-a65c-aeec5c6d2eb4	2014-07-17	Warnings	Exact identifier spl id: b1b6f9cd-d97f-4788-a761-8bc0a9e2ccf6 spl set id: 223814fd-2a5b-4d3f-a65c-aeec5c6d2eb4

Reported adverse events (FAERS/openFDA)#

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