Label: LACTO REMEDY LADYS FOAMING WASH- lactobacillus ferment lysate liquid
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- NDC Code(s): 82892-303-01
- Packager: Body and Co Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 26, 2022
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inactive ingredient
Water, Dipropylene glycol, Coco-Betaine, D- isodium Cocoamphodiacetate, Sodium Chl- oride, Artemisia Princeps Leaf Extract, Ha- mamelis Virginiana (Witch Hazel) Leaf Ext- ract, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Hippophae Rhamnoides Fruit Extr- act, Centella Asiatica Leaf Extract, Camellia Sinensis Leaf Extract, Butylene Glycol, Dis- odium EDTA , Sodium Citrate, Trehalose, P- ropanediol, Zinc Ricinoleate, Tetrasodium G- lutamate Diacetate, Gluconolactone, Allan- toin , 1,2-Hexanediol, Hexylene Glycol, Hy- droxyacetophenone, Caprylyl Glycol, Dipo- tassium Glycyrrhizate, Lauryl Glucoside, Et- hylhexylglycerin
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INGREDIENTS AND APPEARANCE
LACTO REMEDY LADYS FOAMING WASH
lactobacillus ferment lysate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82892-303 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIMOSILACTOBACILLUS FERMENTUM (UNII: BQX4W45LG8) (LIMOSILACTOBACILLUS FERMENTUM - UNII:BQX4W45LG8) LIMOSILACTOBACILLUS FERMENTUM 0.0176 g in 100 g Inactive Ingredients Ingredient Name Strength COCO-BETAINE (UNII: 03DH2IZ3FY) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) CENTELLA ASIATICA LEAF (UNII: 6810070TYD) WATER (UNII: 059QF0KO0R) SODIUM CITRATE (UNII: 1Q73Q2JULR) PROPANEDIOL (UNII: 5965N8W85T) GLUCONOLACTONE (UNII: WQ29KQ9POT) HEXYLENE GLYCOL (UNII: KEH0A3F75J) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) DIPROPYLENE GLYCOL (UNII: E107L85C40) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) SODIUM CHLORIDE (UNII: 451W47IQ8X) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ZINC RICINOLEATE (UNII: BOH1Z111J2) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) ALLANTOIN (UNII: 344S277G0Z) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) TREHALOSE (UNII: B8WCK70T7I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82892-303-01 150 g in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product 07/26/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/26/2022 Labeler - Body and Co Corp. (695702369) Registrant - Body and Co Corp. (695702369)
