Label: COZACO WOMAN- red ginseng tablet
- NDC Code(s): 81651-0002-1
- Packager: Kone Bio Logics 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 10, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Seaweed calcium
Black garlic extract powder
Maca(Lepidium meyenii) extract powder
Oja extract powder
Gigas extract powder
Damiana leaf extract powder
Pumpkin seed extract powder,
Cornifructus(fruit) powder
9 types of Mineral vitamin
Poriacocos powder
Pomegranate extract powder
L-Arginine
L-Teanine
Zinc oxide
Guarane extract powder
Crystalline cellulose
Magnesium stearate
Hydroxypropyl methylcellulose
Nicotinic acid amide
Glycine
L-histidine
Calcium pantothenate
Vitamin B6 Hydrochloride
Folic acid
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
-
WARNING
Please check product ingredients if you have any allergies before taking.
Please be careful during open the product package.
Keep product out of direct sunlight, high temperature and humidity.
Store in a cool dry place.
Any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item.
consult your doctor if any abnormal symptoms occur
- USES
- INDICATION & USAGE SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
COZACO WOMAN
red ginseng tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81651-0002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0) (PANAX GINSENG ROOT OIL - UNII:P9T4K47OM0) PANAX GINSENG ROOT OIL 44.2 Inactive Ingredients Ingredient Name Strength GARLIC OIL (UNII: 4WG8U28833) Product Characteristics Color white Score score with uneven pieces Shape OVAL Size 12mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81651-0002-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/10/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/10/2021 Labeler - Kone Bio Logics Co., Ltd. (695121846) Registrant - Kone Bio Logics Co., Ltd. (695121846) Establishment Name Address ID/FEI Business Operations Kone Bio Logics Co., Ltd. 695121846 manufacture(81651-0002)