BLUE ICE ANALGESIC- menthol gel 
Delon Laboratories (1990) Ltd

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Blue Ice Gel

Active ingredient


Menthol 2.0%

Purpose

Topical analgesic

Uses

Warnings

For external use only

When using this product

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

ammonium hydroxide, carbomer, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate, sodium hydroxide, thymol, water

Delon 8oz (227g)

Delon Blue Ice Gel 8 oz

Penetro 227g

Penetro Blue Ice Analgesic Gel 227 g

BLUE ICE ANALGESIC 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-021
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
THYMOL (UNII: 3J50XA376E)  
AMMONIA (UNII: 5138Q19F1X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)  
CARBOMER 934 (UNII: Z135WT9208)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61734-021-01100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/07/201011/06/2017
2NDC:61734-021-02113.56 g in 1 CONTAINER; Type 0: Not a Combination Product05/07/201012/04/2014
3NDC:61734-021-03227 g in 1 CONTAINER; Type 0: Not a Combination Product05/07/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/07/2010
Labeler - Delon Laboratories (1990) Ltd (248364184)
Establishment
NameAddressID/FEIBusiness Operations
Laboratoires Delon208896216manufacture(61734-021) , pack(61734-021) , label(61734-021)

Revised: 10/2023
Document Id: 0876bc42-b31b-3525-e063-6294a90a510e
Set id: 184ed488-6e62-40c6-bb71-1d523280fd6b
Version: 15
Effective Time: 20231024
 
Delon Laboratories (1990) Ltd