Label: POWER GEMSTONE- ginseng pill
-
Contains inactivated NDC Code(s)
NDC Code(s): 71960-0003-1 - Packager: Myeong SA
- 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 16, 2020
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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
POWER GEMSTONE
ginseng pillProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71960-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PANAX GINSENG WHOLE (UNII: 9L5JEP7MES) (PANAX GINSENG WHOLE - UNII:9L5JEP7MES) PANAX GINSENG WHOLE 20 g in 100 g Inactive Ingredients Ingredient Name Strength MAGNOLIA OFFICINALIS WHOLE (UNII: 9OB542Y2EX) Product Characteristics Color green Score no score Shape OVAL Size 5mm Flavor PEPPERMINT Imprint Code None Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71960-0003-1 300 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/13/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/13/2018 Labeler - Myeong SA (689605005) Registrant - Myeong SA (689605005) Establishment Name Address ID/FEI Business Operations Myeong SA 689605005 manufacture(71960-0003)
