Label: REORGANIC FEMININE WASH- adenosine gel
- NDC Code(s): 82083-0021-1
- Packager: LAON COMMERCE co ltd
- 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 July 4, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
REORGANIC FEMININE WASH
adenosine gelProduct 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)
