FDA.reportPublic FDA data

NattoGrapeSeedEnzymePowder

Manufacturer
Shenzhen Aiwei Biological Technology Co., Ltd.
Effective date
2020-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:13:12

Label at a glance#

ProductNattoGrapeSeedEnzymePowder
Active ingredientORANGE, MALTODEXTRIN, NATTOKINASE, RED YEAST, ASCORBIC ACID, STEM BROMELAIN, ARGININE, VITIS VINIFERA SEED
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

Sucralose, citric acid, 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

Grape seed extract, natto powder, red yeast rice, pinea pple enzyme, vitaminC, Matcha powder, orange powder, litchi powder, soy p eptide powder

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55030-002-022022-01-28C16284748780-1d6a99b39-74ff-a426-e053-dadaa90af4c2a7caf613-f3fc-3d73-e053-2995a90adaf0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55030-002-01NattoGrapeSeedEnzymePowder5 g in 1 PACKAGEPOWDER51
55030-002-02NattoGrapeSeedEnzymePowder15 in 1 PACKAGE, COMBINATIONPOWDER151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55030-002NATTOGRAPESEEDENZYMEPOWDER POWDER [SHENZHEN AIWEI BIOLOGICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 2 package rows20200611_a7caf613-f3fc-3d73-e053-2995a90adaf0.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55030-00255030-002-01, 55030-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ORANGE5EVU04N5QUACTIB
MALTODEXTRIN7CVR7L4A2DACTIB
SUCRALOSE96K6UQ3ZD4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
NATTOKINASEH81695M5OPACTIB
RED YEAST1EU532DCW4ACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
STEM BROMELAINZLM4P8929RACTIB
ARGININE94ZLA3W45FACTIB
VITIS VINIFERA SEEDC34U15ICXAACTIB

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
a7caf454-2364-805b-e053-2a95a90a5a22a7caf613-f3fc-3d73-e053-2995a90adaf02020-06-03WarningsExact identifier
spl id: a7caf454-2364-805b-e053-2a95a90a5a22
spl set id: a7caf613-f3fc-3d73-e053-2995a90adaf0

Reported adverse events (FAERS/openFDA)#

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