BQCELL REVIRGIN GUNG- sodium sulfate tablet

BQCELL REVIRGIN GUNG by

Drug Labeling and Warnings

BQCELL REVIRGIN GUNG by is a Otc medication manufactured, distributed, or labeled by Dermabqcell Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium fulfate

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

feminine cleanser

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

- external use only

- Be careful not to swallow

DOSAGE & ADMINISTRATION

For external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BQCELL REVIRGIN GUNG 
sodium sulfate tablet

Product 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)