LESONEL FORMING FEMININE WASH- methylpropanediol liquid 
ACE PHARMACEUTICAL CO LTD

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.

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Drug Facts

METHYLPROPANEDIOL

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

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 THE CHILDREN

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

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

for vaginal use only

label

LESONEL FORMING FEMININE WASH 
methylpropanediol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74196-0007
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYLPROPANEDIOL (UNII: N8F53B3R4R) (METHYLPROPANEDIOL - UNII:N8F53B3R4R) METHYLPROPANEDIOL0.685 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74196-0007-1300 mL in 1 BOTTLE; Type 0: Not a Combination Product01/18/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/18/2024
Labeler - ACE PHARMACEUTICAL CO LTD (689058677)
Registrant - ACE PHARMACEUTICAL CO LTD (689058677)
Establishment
NameAddressID/FEIBusiness Operations
ACE PHARMACEUTICAL CO LTD689058677manufacture(74196-0007)

Revised: 1/2024
Document Id: 0f2f0ac3-1ff0-c3da-e063-6394a90a2d9f
Set id: 0f2f0ac3-1fef-c3da-e063-6394a90a2d9f
Version: 1
Effective Time: 20240117
 
ACE PHARMACEUTICAL CO LTD