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Ice Cold Analgesic Gel

Medically reviewed by Drugs.com. Last updated on March 5, 2021.

Dosage form: gel
Ingredients: MENTHOL 1g in 100g, CAMPHOR (SYNTHETIC) 0.5g in 100g
Labeler: Universal Distribution Center LLC
NDC Code: 52000-013

Active Ingredients

Menthol             1.0%

Camphor            0.5%

Purpose

Topical Analgesic

Uses

for the temporary relief  of minor aches and pains in muscles and joints associated with:

  • simple backache
  • strains
  • sprains
  • sports injuries
  • arthritis
  • bruises

Warnings

For external use only

Do not use

  • with other topical pain relievers
  • with heating pads or heating devices

When using this product

  • do not use in or near eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask doctor if

  • condition worsens
  • symptoms last more than 7 days or clean up and occur again within a few days
  • redness or irritation develops

If pregnant or breast-feeding, ask a health professional before use

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • clean affected area before applying product
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily

Inactive ingredients

benzyl alcohol, butylated hydroxytoluene, carbopol, colour brillient blue, creasmer RH 40, disodium EDTA, isopropyl alcohol, propylene glycol, purified water and sodium hydroxide

PRINCIPAL DISPLAY PANEL

ICE COLD ANALGESIC GEL

Topical Analgesic
NET WT.8 OZ (227g)



ICE COLD ANALGESIC GEL 
menthol and camphor gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-013
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL1 g  in 100 g
CAMPHOR (SYNTHETIC) (CAMPHOR (SYNTHETIC)) CAMPHOR (SYNTHETIC)0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL 
BUTYLATED HYDROXYTOLUENE 
CARBOMER 934 
FD&C BLUE NO. 1 
EDETATE DISODIUM 
ISOPROPYL ALCOHOL 
PROPYLENE GLYCOL 
SODIUM HYDROXIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:52000-013-17127 g in 1 TUBE
2NDC:52000-013-18170 g in 1 TUBE
3NDC:52000-013-13170 g in 1 BOTTLE, PLASTIC
4NDC:52000-013-14227 g in 1 BOTTLE, PLASTIC
5NDC:52000-013-15300 g in 1 BOTTLE, PLASTIC
6NDC:52000-013-16500 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/15/2013
Labeler - Universal Distribution Center LLC (019180459)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
NameAddressID/FEIOperations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-013)

 
Universal Distribution Center LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.