Label: GELLE-N-DETOX - LAVENDER AND ROSEMARY MASSAGE- benzalkonium chloride lotion
- NDC Code(s): 49283-015-07
- Packager: CHEMCO CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- WARNINGS
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Directions
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Water (Aqua), Paraffinum Liquidum, Cetyl Alcohol, Stearic Acid, 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 LAVENDER & ROSEMARY MASSAGE LOTION 0.7 oz
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INGREDIENTS AND APPEARANCE
GELLE-N-DETOX - LAVENDER AND ROSEMARY MASSAGE
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49283-015 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 CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) COCONUT OIL (UNII: Q9L0O73W7L) ARGAN OIL (UNII: 4V59G5UW9X) DMDM HYDANTOIN (UNII: BYR0546TOW) TROLAMINE (UNII: 9O3K93S3TK) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CETYL ALCOHOL (UNII: 936JST6JCN) SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) LINALOOL, (+/-)- (UNII: D81QY6I88E) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) D&C VIOLET NO. 2 (UNII: 350KA7O6HK) BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69) BENZYL SALICYLATE (UNII: WAO5MNK9TU) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) GERANIOL (UNII: L837108USY) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L) STEARIC ACID (UNII: 4ELV7Z65AP) TRIDECETH-6 (UNII: 3T5PCR2H0C) HYDROXYPROLINE (UNII: RMB44WO89X) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) WATER (UNII: 059QF0KO0R) MINERAL OIL (UNII: T5L8T28FGP) AMINO ACIDS, WHEAT (UNII: 0370GZL32F) PANTHENOL (UNII: WV9CM0O67Z) Product Characteristics Color purple Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49283-015-07 20 g in 1 POUCH; Type 1: Convenience Kit of Co-Package 12/05/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 12/04/2025 Labeler - CHEMCO CORPORATION (032495954) Registrant - CHEMCO CORPORATION (032495954) Establishment Name Address ID/FEI Business Operations CHEMCO CORPORATION 032495954 manufacture(49283-015)

