PHARMACY BEST ICE- menthol gel 
New Pride 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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ACTIVE INGREDIENT:

Menthol, 1.0%

Topical Analgesic

Use

Pharmacy's Best Ice Gel to provide temporary relief of minor pains and aches in your body's joints and muscles associated with:

■ sports injuries ■ sprains ■ arthritis ■ burises

WARNINGS:

For external use only.

Do not apply to wound or damaged skin. Do not bandage the applied surface. Avoid contact with mucous membranes and eyes.

if condition worsens, discontinue use of this product and consult a physician if symptoms persist for more than 7 days.

Do not heat in microwave, add to hot water or any container where heating water may cause splattering and result in burns. Do not use with heating devices or pads.

KEEP OUT OF REACH OF CHILDREN.

In case of accidental ingestion, seek professional advice or contact a Posion Control Center immediately.

DIRECTIONS:

For Adults & Children 2 years & older.

Apply liberally to painful zone and massage until absorbed into the skin. Repeat 3 or 4 times daily. Do not apply to children below two years of age.

INACTIVE INGREDIENTS:

Water (Aqua), Camphor, Ethyl Alcohol, Sodium Hydroxide, Carbomer, Methylchoroisothiazolinone, Methylisothiazolinone, FD&C Blue No. 1.

label

PHARMACY BEST ICE 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58037-204
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
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
WATER (UNII: 059QF0KO0R)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CARBOMER 934 (UNII: Z135WT9208)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58037-204-01227 g in 1 BOTTLE; Type 0: Not a Combination Product04/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/01/2023
Labeler - New Pride Corp (884264198)

Revised: 4/2023
Document Id: f9c153f9-dfb6-5c7e-e053-6294a90a4417
Set id: f9c153f9-dfb5-5c7e-e053-6294a90a4417
Version: 1
Effective Time: 20230401
 
New Pride Corp