ARCTIC ICE ANALGESIC- menthol gel

Arctic Ice Analgesic by

Drug Labeling and Warnings

Arctic Ice Analgesic by is a Otc medication manufactured, distributed, or labeled by Blue Cross Labs, Blue Cross Labs . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:               Purpose

Menthol, 1%  .................. Topical analgesic

PURPOSE

Uses: temporarily relieves:

• minor muscle aches and pains

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Consult a doctor and discontinue use;

if conditon worsens, persists for more than 1 week or tends to recur

WARNINGS

Warnings: For external use only; avoid contact with eyes. Ask a doctor before use if you have associated with

• smoking
• excessive phlegm
• asthma
• emphysema
• persisten or chronic cough

When using this product, do; heat

• microwave
• add to hot water or any container where healing water may cause splatter and result in burns
• use in eyes or directly on mucous membranes
• take by mouth or place in nostrils
• apply to wounds or damaged skin
• bandage skin

DOSAGE & ADMINISTRATION

Directions:

For the temporary relief of minor muscle aches and pains. See important warnings under "When using this product"

• not for use on children under 2 years of age
• adults & children 2 year & older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 time daily.

INACTIVE INGREDIENT

Blue 1, Camphor, Carbomer, Isopropyl Alcohol, Methylchoroisothiazolinone, Methylisothiazolinone, Sodium Hydroxide, Water.

PRINCIPAL DISPLAY PANEL

Arctic Ice

Analgesic Gel

NET WT. 8 OZ. (227)

INGREDIENTS AND APPEARANCE

ARCTIC ICE ANALGESIC 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 22431-600
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
CARBOMER 940 (UNII: 4Q93RCW27E)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 22431-600-01	227 g in 1 JAR; Type 0: Not a Combination Product	09/16/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	09/16/2015

Labeler - Blue Cross Labs (008298879)

Registrant - Blue Cross Labs (008298879)

Establishment
Name	Address	ID/FEI	Business Operations
Blue Cross Labs		008298879	manufacture(22431-600)