Label: LACTO REMEDY LADYS INNER CARE GEL- lactobacillus ferment lysate solution, gel forming / drops
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- NDC Code(s): 82892-304-01
- 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 Ingredients
Water, Butylene Glycol, Methylpropanediol, Hydroxyethylcellulose, Bifida Ferment Lysate, Camellia Sinensis Leaf Extract, Artemisia Princeps Leaf Extract, Centella Asiatica Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Hippophae Rham- noides Fruit Extract, Chamomilla Recutita (Matricaria) Flower Extract, Tre- mella Fuciformis (Mushroom) Extract, Sodium Hyaluronate, Vincetoxicum Atratum Extract, Adenosine, Xanthan Gum, Propanediol, Hydroxyacetoph enone,1,2-Hexanediol, Dipotassium Glycyrrhizate, Citric Acid,Sodium Citr- ate, Dipropylene Glycol
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INGREDIENTS AND APPEARANCE
LACTO REMEDY LADYS INNER CARE GEL
lactobacillus ferment lysate solution, gel forming / dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82892-304 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIMOSILACTOBACILLUS FERMENTUM (UNII: BQX4W45LG8) (LIMOSILACTOBACILLUS FERMENTUM - UNII:BQX4W45LG8) LIMOSILACTOBACILLUS FERMENTUM 0.025 g in 100 g Inactive Ingredients Ingredient Name Strength METHYLPROPANEDIOL (UNII: N8F53B3R4R) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) WATER (UNII: 059QF0KO0R) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) CHAMOMILE (UNII: FGL3685T2X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PROPANEDIOL (UNII: 5965N8W85T) DIPROPYLENE GLYCOL (UNII: E107L85C40) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) ADENOSINE (UNII: K72T3FS567) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) GREEN TEA LEAF (UNII: W2ZU1RY8B0) HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T) TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU) VINCETOXICUM ATRATUM WHOLE (UNII: U3176B0S5J) XANTHAN GUM (UNII: TTV12P4NEE) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ACONITIC ACID (UNII: 93371T1BXP) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82892-304-01 18 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/25/2022 Labeler - Body and Co Corp. (695702369) Registrant - Body and Co Corp. (695702369) Establishment Name Address ID/FEI Business Operations Body and Co Corp. 695702369 manufacture(82892-304)
