ARCTIC ICE PAIN RELIEVING- menthol gel 
Blue Cross Laboratories, Inc.

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.

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ARCTIC ICE pain relieving gel

ARCTIC ICE ANALGESIC GEL


Active Ingredient

Menthol 2.0%

Purpose

Topical Analgesic

Uses

Temporary relief:

minor muscles aches and pains

Warnings


For external use only. Avoid contact with eyes.

Ask a doctor before use if you have cough associated with

When using this product do not

Consult a doctor and discontinue use

if condition worsens, persist for more than 1 week or tends to recur

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

For the temporary relief of minor muscle aches and pains

see important warnings under "When using this product"

Inactive Ingredients

blue 1, camphor, carbomer, isopropyl alcohol, methylchoroisothiazolinone, methuylisothiazoline, sodium hydroxide, water

arctic ice

ARCTIC ICE PAIN RELIEVING 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-014
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:22431-014-011 in 1 PACKAGE02/23/2017
1227 g in 1 JAR; Type 0: Not a Combination Product
2NDC:22431-014-021 in 1 PACKAGE11/11/2020
2198 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/23/2017
Labeler - Blue Cross Laboratories, Inc. (008298879)
Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd (530766098)
Establishment
NameAddressID/FEIBusiness Operations
Ningbo Liyuan Daily Chemical Products Co., Ltd530766098manufacture(22431-014)

Revised: 11/2020
Document Id: b47b5fb7-9b9a-2bc5-e053-2a95a90aa044
Set id: ec805ae9-bd75-4cbd-aa82-714c649790de
Version: 2
Effective Time: 20201119
 
Blue Cross Laboratories, Inc.