Label: GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE- benzalkonium chloride lotion
- NDC Code(s): 49283-110-07
- Packager: CHEMCO CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated September 21, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES:
- WARNINGS
- WHEN USING
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
- OTHER SAFETY INFORMATION
-
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
- GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE LOTION 0.7 oz
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INGREDIENTS AND APPEARANCE
GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE
benzalkonium chloride lotionProduct 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)