BQCELL REVIRGIN GUNG

Manufacturer: Dermabqcell Co., Ltd.
Effective date: 2022-04-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:49:08

Label at a glance#

ProductBQCELL REVIRGIN GUNG

Active ingredientSODIUM SULFATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium fulfate

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

feminine cleanser

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

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 SECTION

- external use only

- Be careful not to swallow

DOSAGE & ADMINISTRATION SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
d676a241-be05-4740-b3ee-1a5f2ed422d2	Product name	4	20180615
dd8bd48f-20d6-43c7-b471-3ae872868afa	Product name	3	20180125
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
d41954ff-bc63-4b2c-aba0-9146707659d7	Product name	2	20151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
82665-0001-1	2024-01-30	C162847	48780-1	1030e364-f976-111a-e063-dadaa90a10e2	dc2fc056-645e-1c96-e053-2a95a90aa6be

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82665-0001-1	BQCELL REVIRGIN GUNG	1 in 1 POUCH	TABLET	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82665-0001	BQCELL REVIRGIN GUNG (SODIUM SULFATE) TABLET [DERMABQCELL CO., LTD.]	1	Legacy NDC, 1 package rows	20220409_dc2fc056-645e-1c96-e053-2a95a90aa6be.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

BQCELL REVIRGIN GUNG
Sodium Sulfate
NIACINAMIDE
ADENOSINE
SODIUM SULFATE ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82665-0001	82665-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
NIACINAMIDE	25X51I8RD4	IACT
ADENOSINE	K72T3FS567	IACT
SODIUM SULFATE	0YPR65R21J	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
dc2fbfd7-b2e4-f8d5-e053-2995a90aa2de			dc2fc056-645e-1c96-e053-2a95a90aa6be	2022-04-08	Warnings	Exact identifier spl id: dc2fbfd7-b2e4-f8d5-e053-2995a90aa2de spl set id: dc2fc056-645e-1c96-e053-2a95a90aa6be

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.