Label: ROBONGBANG PROPOLIS- propolis capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 76254-2001-1 - Packager: Seoul Propolis
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 28, 2017
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ROBONGBANG PROPOLIS
propolis capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76254-2001 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF) PROPOLIS WAX 85 mg Inactive Ingredients Ingredient Name Strength SOYBEAN (UNII: L7HT8F1ZOD) VITIS VINIFERA SEED (UNII: C34U15ICXA) WHITE WAX (UNII: 7G1J5DA97F) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0) GARLIC (UNII: V1V998DC17) ASCORBIC ACID (UNII: PQ6CK8PD0R) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) 1-OCTACOSANOL (UNII: 81I2215OVK) TAURINE (UNII: 1EQV5MLY3D) Product Characteristics Color brown (dark brown) Score no score Shape ROUND (tablet) Size 15mm Flavor Imprint Code 3;hp;x Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76254-2001-1 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/28/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/16/2011 Labeler - Seoul Propolis (687390351) Registrant - Seoul Propolis (687390351) Establishment Name Address ID/FEI Business Operations Seoul Propolis Co., Ltd. 687390351 manufacture(76254-2001)