Label: BLACKCURRANTENZYMEPOWDER powder
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Contains inactivated NDC Code(s)
NDC Code(s): 55030-003-01, 55030-003-02 - Packager: Shenzhen Aiwei Biological Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated June 11, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- ACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLACKCURRANTENZYMEPOWDER
blackcurrantenzymepowder powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55030-003 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength .BETA.-CAROTENE (UNII: 01YAE03M7J) (.BETA.-CAROTENE - UNII:01YAE03M7J) .BETA.-CAROTENE 0.36 g in 3 g KERACYANIN (UNII: V0N2VMB4FV) (KERACYANIN - UNII:V0N2VMB4FV) KERACYANIN 0.45 g in 3 g LUTEIN (UNII: X72A60C9MT) (LUTEIN - UNII:X72A60C9MT) LUTEIN 0.6 g in 3 g .BETA.-CAROTENE, (9Z)- (UNII: 3K5NFW97PV) (.BETA.-CAROTENE, (9Z)- - UNII:3K5NFW97PV) .BETA.-CAROTENE, (9Z)- 0.45 g in 3 g STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V) STRAWBERRY 0.3 g in 3 g MALTODEXTRIN (UNII: 7CVR7L4A2D) (MALTODEXTRIN - UNII:7CVR7L4A2D) MALTODEXTRIN 0.3 g in 3 g CRANBERRY (UNII: 0MVO31Q3QS) (CRANBERRY - UNII:0MVO31Q3QS) CRANBERRY 0.36 g in 3 g Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ASCORBIC ACID (UNII: PQ6CK8PD0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55030-003-02 15 in 1 PACKAGE, COMBINATION 06/03/2020 1 NDC:55030-003-01 3 g in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/03/2020 Labeler - Shenzhen Aiwei Biological Technology Co., Ltd. (550302337) Establishment Name Address ID/FEI Business Operations Shenzhen Aiwei Biological Technology Co., Ltd. 550302337 manufacture(55030-003)
