FDA.reportPublic FDA data

PHARMACYS PRESCRIPTION ICE COLD ANALGESIC

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2018-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:45:10

Label at a glance#

ProductPHARMACYS PRESCRIPTION ICE COLD ANALGESIC
Active ingredientMENTHOL
Label structure11 sections

Indications and uses

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

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

Storage and handling

Do Not Freeze

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1 percent

Purpose

OTC - PURPOSE SECTION

Pain relieving gel

Uses:

DOSAGE & ADMINISTRATION SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not handage tightly
  • do not apply to wounds or damaged skin
  • do not use with heating pads or other heating devices

Stop use and ask doctor if

OTC - STOP USE SECTION

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days. (see other side panel)

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Posion Control Center immediately.

Directions

INDICATIONS & USAGE 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

Other Information

STORAGE AND HANDLING SECTION

Do Not Freeze

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-11376176-113-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
CARBOMER 934Z135WT9208IACT
MENTHOLL7T10EIP3AACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
77135be8-93fe-9f5e-e053-2991aa0a093b77135be8-93fd-9f5e-e053-2991aa0a093b2018-08-01WarningsExact identifier
spl id: 77135be8-93fe-9f5e-e053-2991aa0a093b
spl set id: 77135be8-93fd-9f5e-e053-2991aa0a093b

Reported adverse events (FAERS/openFDA)#

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