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

GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE by

Drug Labeling and Warnings

GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE by is a Otc medication manufactured, distributed, or labeled by CHEMCO CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

PURPOSE

Antimicrobial

USES:

To decrease bacteria on the skin.

WARNINGS

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.

WHEN USING

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

ASK DOCTOR

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

PREGNANCY 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:

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

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

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.

QUESTIONS

Call (305) 623-4445

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)
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
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)