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

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

PURPOSE

Antibacterial

USES:

To decrease bacteria on the skin.

DIRECTIONS:

Apply product on hands, feet, body as needed. Rub hands together
until absorbed.

WARNINGS

For external use only.

WHEN USING

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

KEEP OUT OF REACH OF CHILDREN

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

INACTIVE INGREDIENT

Aqua, Paraffinum Liquidum, Stearic Acid, Cetyl Alcohol, Stearyl
Alcohol, Parfum, DMDM Hydantoin, Triethanolamine,
Acrylamide/Sodium Acrylate Copolymer, Trideceth-6,
Methylparaben, Propylparaben, Cocos Nucifera Oil (Organic),
Argania Spinosa Kernel Oil (Organic), Methyl Salicylate,
Eucalyptus Globulus Leaf Oil, Sodium Hyaluronate, Sodium PCA,
Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey)
Extract, Hydroxyproline, FD&C Yellow #5 (CI 19140), FD&C Blue
MASSAGE LOTION #1 (CI 42090), Citral, D-Limonene, Geraniol, Linalool.

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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)
ARGAN OIL (UNII: 4V59G5UW9X)
EUCALYPTUS OIL (UNII: 2R04ONI662)
MINERAL OIL (UNII: T5L8T28FGP)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PANTHENOL (UNII: WV9CM0O67Z)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLPARABEN (UNII: A2I8C7HI9T)
DMDM HYDANTOIN (UNII: BYR0546TOW)
HYDROXYPROLINE (UNII: RMB44WO89X)
COCONUT OIL (UNII: Q9L0O73W7L)
GERANIOL (UNII: L837108USY)
LINALOOL, (+)- (UNII: F4VNO44C09)

Product Characteristics
Color	green (Light green)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49283-110-07	20 g in 1 POUCH; Type 1: Convenience Kit of Co-Package	01/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/19/2023

Labeler - CHEMCO CORPORATION (032495954)

Registrant - CHEMCO CORPORATION (032495954)

Establishment
Name	Address	ID/FEI	Business Operations
CHEMCO CORPORATION		032495954	manufacture(49283-110)