Label: LA FEMME V FEMININE CLEANSER- olea europaea leaf, myrrh, niacinamide tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 72798-010-01, 72798-010-02 - Packager: Nature Factory 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 January 30, 2019
If you are a consumer or patient please visit this version.
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Sodium Sulfate, Sophora Flavescens Extract, Camellia Sinensis Leaf Extract, Centella Asiatica Extract, Paeonia Lactiflora Extract, Glycyrrhiza Uralensis (Licorice) Root Extract, Iris Ensata Extract, Artemisia Princeps Extract, Aloe Barbadensis Extract, Menthol, Turpentine, Kaolin, Adenosine, Hydroxypropyl Methylcellulose, Magnesium stearate - PURPOSE
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WARNINGS
Warnings:
Keep out of reach of children
Because the product supplies nutrition to vagina, the latent harmful bacteria may be activated if using the product for consecutive days, causing a temporary vaginal discharge and itching. For such case, please stop using the product and discuss with physician for continued uses.
(recommended to treat spouse together) However, if you have itchy based on chronic vaginosis, please desire not to use it. - KEEP OUT OF REACH OF CHILDREN
- Uses
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Directions
Directions:
1.Use it at bedtime preferably or during daytime without dynamic activities.2.Wash your finger and insert 1 tablet into the vagina with first two knuckles of a finger.
3.It will take 20-30 minutes until the tablet is dissolved to relieve the symptoms and clean the vagina. 4.Do not use within 6 hours prior to vaginal intercourse.
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LA FEMME V FEMININE CLEANSER
olea europaea leaf, myrrh, niacinamide tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72798-010 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) (OLEA EUROPAEA LEAF - UNII:MJ95C3OH47) OLEA EUROPAEA LEAF 8.0 mg in 800 mg MYRRH (UNII: JC71GJ1F3L) (MYRRH - UNII:JC71GJ1F3L) MYRRH 8.0 mg in 800 mg NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 16.0 mg in 800 mg Inactive Ingredients Ingredient Name Strength Sodium Sulfate (UNII: 0YPR65R21J) Product Characteristics Color white Score no score Shape OVAL Size 15mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72798-010-02 5 in 1 CARTON 12/01/2018 1 NDC:72798-010-01 800 mg in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2018 Labeler - Nature Factory Co., Ltd. (689517404) Registrant - Nature Factory Co., Ltd. (689517404) Establishment Name Address ID/FEI Business Operations Chebigen Co.,ltd. 688847594 manufacture(72798-010)
