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FDA Approval

Hankki ssog Pre-Biome Shake (Detox and Diet Shake)

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
BIOHERB Co., Ltd.
DUNS: 695625893
Effective Date
May 28, 2025
Labeling Type
HUMAN OTC DRUG LABEL
pea fiber(5 g in 100 g)
Lactic acid(10 g in 100 g)
Cotton(5 g in 100 g)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

BIOHERB Co., Ltd.

BIOHERB Co., Ltd.

695625893

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Hankki ssog Pre-Biome Shake (Detox and Diet Shake)

Product Details

NDC Product Code
77008-5712
Route of Administration
TOPICAL
Effective Date
May 28, 2025
pea fiberActive
Code: KF5Q0VDK1NClass: ACTIBQuantity: 5 g in 100 g
WATERInactive
Code: 059QF0KO0RClass: IACTQuantity: 1 g in 100 g
Code: 33X04XA5ATClass: ACTIBQuantity: 10 g in 100 g
CottonActive
Code: 70LDW53ROOClass: ACTIBQuantity: 5 g in 100 g

Drug Labeling Information

Complete FDA-approved labeling information including indications, dosage, warnings, contraindications, and other essential prescribing details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ssog


RECENT MAJOR CHANGES SECTION


INDICATIONS & USAGE SECTION

Fluids metabolism smooth

Blood metabolism smooth

Reducing body fat

Elimination of waste in blood

Remove swelling

Acquiring gastrointestinal satisfaction

Reducing food intake

DOSAGE & ADMINISTRATION SECTION


WARNINGS SECTION

Warning: For adult-use only


OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Improves hair-loss

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN.


INACTIVE INGREDIENT SECTION


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