Label: MEORI TOKTOK- biotinm propolis liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 83125-0001-1 - Packager: Kolive Cell Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 26, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEORI TOKTOK
biotinm propolis liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83125-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 0.5 g in 100 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.2 g in 100 mL Inactive Ingredients Ingredient Name Strength SULFUR (UNII: 70FD1KFU70) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83125-0001-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/22/2022 Labeler - Kolive Cell Co., Ltd. (695293236) Registrant - Kolive Cell Co., Ltd. (695293236) Establishment Name Address ID/FEI Business Operations Kolive Cell Co., Ltd. 695293236 manufacture(83125-0001)
