PHARMACYS PRESCRIPTION ANALGESIC GEL- menthol gel 
American Consumer Products Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Pharmacy's Prescription 8OZ Ice Cold Analgesic Gel

Active Ingredient

Active Ingredient: Menthol 1%

Purpose

Purpose: Pain relieving gel

Warnings

Warnings: For external use only

Stop Use

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

Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

Inactive Ingredients

Inactive Ingredients

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

Indications & Usage Section

Uses: For the temporary relief of minor aches and pains of muscles and joints associated with - simple backache - arthritis - strains - bruses - sprains

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

Dosage & Administration

Directions

- adults and childrent 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

Pharmacy's Prescription 8 OZ Ice Cold Analgesic Gel

Pharmacys Prescription 8 OZ Ice Cold Analgesic

PHARMACYS PRESCRIPTION ANALGESIC GEL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72197-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
CAMPHOR, (-)- (UNII: 213N3S8275)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
2,2',3,3',4,4',5,5',6-NONACHLORODIPHENYL ETHER (UNII: 4S0765P9W8)  
TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72197-001-08227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34608/31/2018
Labeler - American Consumer Products Corp (081101181)

Revised: 5/2023
Document Id: fb49a6db-2e15-6514-e053-6294a90a3310
Set id: 6f0725f2-833f-f3a0-e053-2a91aa0a3911
Version: 3
Effective Time: 20230509
 
American Consumer Products Corp