REORGANIC FEMININE WASH- adenosine gel

Reorganic Feminine wash by

Drug Labeling and Warnings

Reorganic Feminine wash by is a Otc medication manufactured, distributed, or labeled by LAON COMMERCE co ltd, LAON COMMERCE CO Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lactobacillus crispatus

INACTIVE INGREDIENT

Water
Sodium C14-16 Olefin Sulfonate
Glycerin
Coco-Betaine
Lauryl Hydroxysultaine
Sodium Chloride
Panthenol
Citric Acid
Dipropylene Glycol
Caprylyl Glycol
Hydroxyacetophenone
1,2-Hexanediol
Disodium EDTA
Lactobacillus Ferment
Butylene Glycol
Collagen Extract
Arginine
Glyceryl Caprylate
Decylene Glycol
Madecassoside
Madecassic Acid
Centella Asiatica Extract
Sodium Surfactin
Sodium Stearoyl Glutamate
Asiaticoside
Asiatic Acid
Isopentyldiol
Polyglyceryl-4 Oleate
Propanediol
Polyquaternium-10
Fragrance

PURPOSE

skin protect

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Take an appropriate amount of this product, lather it up, massage it gently, and then wash it off with water

WARNINGS

Precautions for use 1. Consult a specialist, etc. if there are abnormal symptoms or side effects such us red spots, swelling, or itching in the area of use due to direct sunlight when using or after using cosmetics. 2. Refrain from using on areas with wo unds. 3. Precaution for storage and handling a) Keep outof reach of children b) Store away from direct sunlight

DOSAGE & ADMINISTRATION

topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

REORGANIC FEMININE WASH 
adenosine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82083-0021
Route of Administration	VAGINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTOBACILLUS CRISPATUS (UNII: QX2H2M2084) (LACTOBACILLUS CRISPATUS - UNII:QX2H2M2084)	LACTOBACILLUS CRISPATUS	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CENTELLA ASIATICA (UNII: 7M867G6T1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82083-0021-1	200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2023

Labeler - LAON COMMERCE co ltd (557839830)

Registrant - LAON COMMERCE co ltd (557839830)

Establishment
Name	Address	ID/FEI	Business Operations
LAON COMMERCE CO Ltd		557839830	manufacture(82083-0021) , label(82083-0021)