Label: BQCELL REVIRGIN GUNG- sodium sulfate tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 82665-0001-1 - Packager: Dermabqcell 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 April 8, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Collagen
Niacinamide
Olea Europaea (Olive) Leaf Extract
Commiphora Myrrha Resin Extract
Lactobacillus
Adenosine
Magnesium stearate
Leontopodium Alpinum Flower Extract
Sophora Flavescens Root Extract
Quercus Infectoria (Oak) Gall Extract
Cymbopogon Citratus Extract
Chamomilla Recutita (Matricaria) Extract
Gleditsia Australis Thorn Extract
Monarda Didyma Leaf Extract
Phellodendron Amurense Bark Extract
Paeonia Albiflora Root Extract
Cnidium Officinale Root Extract
Hydroxypropyl Methylcellulose
Carthamus Tinctorius (Safflower) Flower Extract
Taraxacum Officinale (Dandelion) Extract
Artemisia Princeps Leaf Extract
Camellia Sinensis Leaf Extract
Centella Asiatica Extract
Acorus Calamus Root Extract
Artemisia Vulgaris Extract
Aloe Barbadensis Leaf Extract
Bifidobacterium
Zinc Oxide - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
1. Cut the pouch and take out the pill-like contents.
2. Dissolve 1 pill in 50cc of water and use it as if massaging around the vulva.
3. When using it for the first time, it is recommended to use it every day for 2-3 days. After that, it is recommended to use once a week on average (except during pregnancy and menstrual period)
4. The effect is better if you learn the proper usage and cycle according to individual differences. - WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BQCELL REVIRGIN GUNG
sodium sulfate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82665-0001 Route of Administration ENTERAL, VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE 0.235 g Inactive Ingredients Ingredient Name Strength NIACINAMIDE (UNII: 25X51I8RD4) ADENOSINE (UNII: K72T3FS567) Product Characteristics Color yellow Score no score Shape ROUND Size 10mm Flavor Imprint Code none Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82665-0001-1 1 in 1 POUCH; Type 0: Not a Combination Product 04/09/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/09/2022 Labeler - Dermabqcell Co., Ltd. (695556088) Registrant - Dermabqcell Co., Ltd. (695556088) Establishment Name Address ID/FEI Business Operations Dermabqcell Co., Ltd. 695556088 manufacture(82665-0001)
