LACTO REMEDY LADYS FOAMING WASH- lactobacillus ferment lysate liquid

LACTO REMEDY Ladys foaming wash by

Drug Labeling and Warnings

LACTO REMEDY Ladys foaming wash by is a Otc medication manufactured, distributed, or labeled by Body and Co Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

Lactobacillus Ferment Lysate 0.01%

purpose

BACTERIOSTATIC

use

Maintain your natural pH balance and keep your intimate area moist.

warnings

Do not suitable for c- hildren under 3 years of age

warnings

This product is for external use only, not e- dible. Women in gestational periods should better not use it and not use it on the vulv- a just before delivery.

warnings

Stop use and ask a doctor if irritation, rash, red spot on the skin, or swelling occurs. These may be signs of a severe
condition.

warnings

Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Take the tissue out of the pouch. Wipe the are from front to back. Throw tissues in the toilet.

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

This product is for external use only, not edible.

label

LACTO REMEDY lady's foaming wash 82892-303

INGREDIENTS AND APPEARANCE

LACTO REMEDY LADYS FOAMING WASH 
lactobacillus ferment lysate liquid

Product 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)