Label: RITE AID COOL THERAPY GEL- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-4217-1 - Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 26, 2022
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- Drug Facts
- Active Ingredients
- Uses
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Warnings
For external use only
When using this product:
Avoid contact with the eyes or mucous membranes; Do not apply to wounds or damaged skin; Do not use with other ointments, creams, sprays or liniments; Do not apply to irritated skin or if excessive irritated develops; Do not bandage; Wash hands after use with cool water; Do not use with a heating pad or device
- Directions
- Inactive Ingredients
- Questions or Comments
- Package Labeling:
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INGREDIENTS AND APPEARANCE
RITE AID COOL THERAPY GEL
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-4217 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CARBOMER 940 (UNII: 4Q93RCW27E) EDETATE DISODIUM (UNII: 7FLD91C86K) DMDM HYDANTOIN (UNII: BYR0546TOW) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ISOPROPYL ALCOHOL (UNII: ND2M416302) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-4217-1 88.72 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/01/2022 Labeler - Rite Aid (014578892) Establishment Name Address ID/FEI Business Operations Anicare Pharmaceuticals Pvt. Ltd. 916837425 manufacture(11822-4217)