Label: CURETECH COLD ICE ANALGESIC GEL- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73622-3021-2 - Packager: Curetech Skincare
- 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 September 28, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses:
- Warnings
- When using this product
- Stop use and ask a doctor if
- If pregnant or breastfeeding
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CURETECH COLD ICE ANALGESIC GEL
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73622-3021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 4.54 g in 227 g Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CUPRIC SULFATE (UNII: LRX7AJ16DT) THYMOL (UNII: 3J50XA376E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73622-3021-2 227 g in 1 JAR; Type 0: Not a Combination Product 04/08/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 04/08/2019 Labeler - Curetech Skincare (677682180)