LESONEL FORMING FEMININE WASH- methylpropanediol liquid

LESONEL FORMING FEMININE WASH by

Drug Labeling and Warnings

LESONEL FORMING FEMININE WASH by is a Otc medication manufactured, distributed, or labeled by ACE PHARMACEUTICAL CO LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

METHYLPROPANEDIOL

INACTIVE INGREDIENT

Water
Disodium Cocoamphodiacetate
Decyl Glucoside
Sodium Chloride
1,2-Hexanediol
Butylene Glycol
Hexylene Glycol
Lactobacillus/Soybean Ferment Extract
Streptococcus Thermophilus Ferment
Bifida Ferment Lysate
Lactobacillus Ferment Lysate
Hydrogenated Lecithin
Ceramide NP
Allantoin
Trehalose
Betaine
Sodium PCA
Citric Acid
Disodium EDTA
Caprylyl Glycol
Ethylhexylglycerin
Steareth-30

PURPOSE

The product, made from naturally derivedsafesurfactants, effectively maintains cleanliness and moisturein the external genital area,

providingarefreshing cleansing sensation without causing irritation

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

Dispense an adequate amount onto the palm of your hand, then gently massage and spread the rich creamy lather before rinsing thoroughly with water.

WARNINGS

1. If you notice any unusual symptoms or side effects such as redness, swelling, or itching in the area where the cos metic product was applied, particularly after direct sunlight expo sure during or after use, seek advice from a specialist or health care professional

2. Do not apply on broken or irritated skin.

3. Precautions for Safe Handling: a. Keep out of reach of children

DOSAGE & ADMINISTRATION

for vaginal use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LESONEL FORMING FEMININE WASH 
methylpropanediol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74196-0007
Route of Administration	VAGINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYLPROPANEDIOL (UNII: N8F53B3R4R) (METHYLPROPANEDIOL - UNII:N8F53B3R4R)	METHYLPROPANEDIOL	0.685 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74196-0007-1	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/18/2024

Labeler - ACE PHARMACEUTICAL CO LTD (689058677)

Registrant - ACE PHARMACEUTICAL CO LTD (689058677)

Establishment
Name	Address	ID/FEI	Business Operations
ACE PHARMACEUTICAL CO LTD		689058677	manufacture(74196-0007)