Label: PHARMACY BEST ICE- menthol gel
- NDC Code(s): 58037-204-01
- Packager: New Pride Corp
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated April 1, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT:
- PURPOSE
- Use
- WARNINGS:
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN.
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PHARMACY BEST ICE
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58037-204 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1 g in 100 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:58037-204-01 227 g in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/01/2023 Labeler - New Pride Corp (884264198)