FDA.reportPublic FDA data

BlackcurrantEnzymePowder

Manufacturer
Shenzhen Aiwei Biological Technology Co., Ltd.
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:12

Label at a glance#

ProductBlackcurrantEnzymePowder
Active ingredient.BETA.-CAROTENE, KERACYANIN, LUTEIN, .BETA.-CAROTENE, (9Z)-, STRAWBERRY, MALTODEXTRIN, CRANBERRY
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

4g/bag, 1 bag a day

WARNINGS SECTION

Please keep out of the reach of children

INACTIVE INGREDIENT SECTION

Citric acid , sucralose , silica

INDICATIONS & USAGE SECTION

: 2 times a day, 1-2 sachets each time, open the bag to eat or take it with warm water, or add it to juice and drinks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Replenish the protein needed by the body

OTC - ACTIVE INGREDIENT SECTION

sorbitol, blueberry powder, black soybean powder, blackcurrant powder, citric acid, DL malic acid,
Lutein fat, a-cyclodextrin, soybean peptide powder

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55030-003-022022-01-28C16284748780-1d6a99b39-5ad1-a426-e053-dadaa90af4c2a7cbc688-6b94-f2a8-e053-2995a90aa414

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55030-003-01BlackcurrantEnzymePowder3 g in 1 PACKAGEPOWDER31
55030-003-02BlackcurrantEnzymePowder15 in 1 PACKAGE, COMBINATIONPOWDER151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55030-003BLACKCURRANTENZYMEPOWDER POWDER [SHENZHEN AIWEI BIOLOGICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 2 package rows20200611_a7cbc688-6b94-f2a8-e053-2995a90aa414.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55030-00355030-003-01, 55030-003-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICON DIOXIDEETJ7Z6XBU4IACT
ASCORBIC ACIDPQ6CK8PD0RIACT
.BETA.-CAROTENE01YAE03M7JACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
KERACYANINV0N2VMB4FVACTIB
LUTEINX72A60C9MTACTIB
.BETA.-CAROTENE, (9Z)-3K5NFW97PVACTIB
STRAWBERRY4J2TY8Y81VACTIB
MALTODEXTRIN7CVR7L4A2DACTIB
CRANBERRY0MVO31Q3QSACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a7cbc688-6b95-f2a8-e053-2995a90aa414a7cbc688-6b94-f2a8-e053-2995a90aa4142020-06-11WarningsExact identifier
spl id: a7cbc688-6b95-f2a8-e053-2995a90aa414
spl set id: a7cbc688-6b94-f2a8-e053-2995a90aa414

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.