Skip to Content

Good Neighbor Pharmacy Therapeutic Blue

Medically reviewed on Jul 23, 2018

Dosage form: gel
Ingredients: MENTHOL 2g in 100g
Labeler: AmerisourceBergen Drug Corporation
NDC Code: 24385-225

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.

Good Neighbor Pharmacy Therapeutic Blue

Drug Facts

Active Ingredients

Active ingredient

Menthol 2%

pain relieving gel

Uses

for the temporary relief of minor aches and

pains of muscles and joints associated with

• simple backache • arthritis • strains

• bruises • sprains

warnings

For external use only

when using this product

• avoid contact with the eyes

• do not bandage tightly

• do not apply to wounds or damaged skin

• do not use with heating pads or other heating devices

Stop using and ask a 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 the reach of children

If swallowed get medical help or contact a Poison Control Center.

Directions

• 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

Inactive Ingredients

Ammonium Hydroxide, Carbomer, Cupric Sulfate, FD&C Blue No. 1,

Isopropyl Alcohol, Magnesium Sulfate,

Sodium Hydroxide, Thymol, Water.

This product is not manufactured by Novartis Consumer

Health, Inc., owner of the registered trademark Mineral Ice®.

GOOD NEIGHBOR PHARMACY THERAPEUTIC BLUE 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-225
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
AMMONIA 
CARBOMER 934 
CUPRIC SULFATE 
FD&C BLUE NO. 1 
ISOPROPYL ALCOHOL 
MAGNESIUM SULFATE 
SODIUM HYDROXIDE 
THYMOL 
WATER 
Packaging
#Item CodePackage Description
1NDC:24385-225-40227 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/11/1988
Labeler - AmerisourceBergen Drug Corporation (007914906)
Establishment
NameAddressID/FEIOperations
Product Quest Mfg, LLC927768135manufacture(24385-225), label(24385-225)

 
AmerisourceBergen Drug Corporation

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide