Label: LACTOMEDI LADYS FOAMING WASH- lactobacillus ferment lysate liquid
- NDC Code(s): 83490-313-01
- Packager: 2359 US INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 25, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- active ingredient
- purpose
- use
- warnings
- warnings
- warnings
- warnings
- Directions
-
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
- WARNINGS
- label
-
INGREDIENTS AND APPEARANCE
LACTOMEDI LADYS FOAMING WASH
lactobacillus ferment lysate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83490-313 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:83490-313-01 150 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 - 2359 US INC (118974080) Registrant - 2359 US INC (118974080)
