Label: ARCTIC ICE ANALGESIC- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 22431-012-01 - Packager: Blue Cross Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 December 26, 2019
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- Official Label (Printer Friendly)
- ARCTIC ICE ANALGESIC GEL
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product do not
- Consult a doctor and discontinue use
- Keep out of reach of children.
- Directions
- Inactive Ingredients
- Principle display panel
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INGREDIENTS AND APPEARANCE
ARCTIC ICE ANALGESIC
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:22431-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.0 g in 100 g Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) ALCOHOL (UNII: 3K9958V90M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ISOPROPYL ALCOHOL (UNII: ND2M416302) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:22431-012-01 227 g in 1 JAR; Type 0: Not a Combination Product 12/11/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/11/2015 Labeler - Blue Cross Laboratories, Inc. (008298879) Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd (530766098) Establishment Name Address ID/FEI Business Operations Ningbo Liyuan Daily Chemical Products Co., Ltd 530766098 manufacture(22431-012)