GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE- benzalkonium chloride lotion 
CHEMCO CORPORATION

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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49283-110-07

Benzalkonium Chloride 0.1%

Antimicrobial

USES:

To decrease bacteria on the skin.

For external use only.

Do not use on wounds or damaged skin, with a heating pad or on a child under 12 years of age.

•Avoid contact with the eyes.
• Do not apply to the irritated skin or if excessive irritation develops.

Ask a doctor before use if you have redness over affected area.

Ask a health professional before use.

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

DIRECTIONS:

Apply a full-palm amount or as needed to cover the affected area (hands, feet, body). Rub until absorbed.

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

Water (Aqua), Paraffinum Liquidum, Stearic Acid, Cetyl Alcohol, Fragrance (Parfum), Stearyl Alcohol, DMDM Hydantoin, Triethanolamine, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Methylparaben, Propylparaben, Cocos Nucifera Oil (Organic), Argania Spinosa Kernel Oil (Organic), Lavandula Angustifolia (Lavender) Extract, Rosmarinus Officinalis (Rosemary) Extract, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, D&C Violet No.2 (CI 60730), Benzyl Salicylate, Linalool, Hexyl Cinnamal, Alpha Isomethyl Ionone, Citronellol, Geraniol.

Call (305) 623-4445


GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE LOTION 0.7 oz

ANTIBACTERIAL LOTION MINT

GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE 
benzalkonium chloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49283-110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CITRAL (UNII: T7EU0O9VPP)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
PANTHENOL (UNII: WV9CM0O67Z)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
MINERAL OIL (UNII: T5L8T28FGP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ARGAN OIL (UNII: 4V59G5UW9X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
COCONUT OIL (UNII: Q9L0O73W7L)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
HYDROXYPROLINE (UNII: RMB44WO89X)  
GERANIOL (UNII: L837108USY)  
LINALOOL, (+)- (UNII: F4VNO44C09)  
Product Characteristics
Colorgreen (Light green) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49283-110-0720 g in 1 POUCH; Type 1: Convenience Kit of Co-Package01/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/19/2023
Labeler - CHEMCO CORPORATION (032495954)
Registrant - CHEMCO CORPORATION (032495954)
Establishment
NameAddressID/FEIBusiness Operations
CHEMCO CORPORATION032495954manufacture(49283-110)

Revised: 9/2023
Document Id: 05e115a5-4d49-43d6-e063-6294a90a07c5
Set id: f2a107aa-5ad3-7bad-e053-2a95a90a1d97
Version: 2
Effective Time: 20230921
 
CHEMCO CORPORATION