FDA.reportPublic FDA data

NIWEDAH SEA MOSS BLACK

Manufacturer
Shenzhen Xiaomai Manufacturing Co., Ltd.
Effective date
2024-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:03:05

Label at a glance#

ProductNIWEDAH SEA MOSS BLACK
Active ingredientARCTIUM LAPPA ROOT, ASCORBIC ACID, TURMERIC, FUCUS VESICULOSUS, NIGELLA SATIVA SEED OIL, CHONDRUS CRISPUS, PREVITAMIN D3, WITHANIA SOMNIFERA WHOLE
Label structure13 sections

Dosage and administration

As a dietary supplement, take two (2) capsulesdaily, or as directed by your health care professional.

Storage and handling

Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Vitamin C

Vitamin D3

Sea Moss

Ashwagandha

Black Seed

Purpose

OTC - PURPOSE SECTION

dietary fiber supplements

Use

INDICATIONS & USAGE SECTION

SUGGESTED USE : As a dietary supplement, take two (2)capsulesdaily, or as directed by your health care professional.

Warnings

WARNINGS SECTION

-For external use only
-Keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

CAUTlON : Do not exceed the recommended dose. Pregnant ornursing mothers, children under the age of 18, and individuals witha known medical condition should consult a physician before usingthis or any dietary supplement.

When Using

OTC - WHEN USING SECTION

Do not exceed the recommended dose. Pregnant ornursing mothers, children under the age of 18, and individuals witha known medical condition should consult a physician before usingthis or any dietary supplement.

Stop Use

OTC - STOP USE SECTION

Do not exceed the recommended dose. Pregnant ornursing mothers, children under the age of 18, and individuals witha known medical condition should consult a physician before usingthis or any dietary supplement.

Ask Doctor

OTC - ASK DOCTOR SECTION

Do not exceed the recommended dose. Pregnant ornursing mothers, children under the age of 18, and individuals witha known medical condition should consult a physician before usingthis or any dietary supplement.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Oot Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

As a dietary supplement, take two (2) capsulesdaily, or as directed by your health care professional.

Other information

STORAGE AND HANDLING SECTION

Before use, read all information on thecarton Store at controlled room temperature20 to 25 C (68 to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Apple Cider Vinegar (Malus domestica)(Fruit) Powder, Dandelion (Taraxacumofficinale) (Root) Extract, Yellow Dock (Rumex crispus) (Root) Powder, Elderberry(Sambucus williamsii hance) (Fruit) xtract, Manuka Honey (Leptospermumscoparium)(Root)Powder, Ginger (Zingiber officinale), Chlorophyll.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83872-136NIWEDAH SEA MOSS BLACK (SEA MOSS BLACK) CAPSULE [SHENZHEN XIAOMAI MANUFACTURING CO., LTD.]1Unmatched20240509_17e33680-1767-e957-e063-6394a90a95e2.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
83872-13683872-136-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARCTIUM LAPPA ROOT597E9BI3Z3ACTIB
ASCORBIC ACIDPQ6CK8PD0RACTIB
TURMERIC856YO1Z64FACTIB
PIPER NIGRUM WHOLE49L10LI8DNIACT
FUCUS VESICULOSUS535G2ABX9MACTIB
NIGELLA SATIVA SEED OILCS4U38E731ACTIB
CHONDRUS CRISPUSOQS23HUA1XACTIB
PREVITAMIN D3HDA46400N5ACTIB
WITHANIA SOMNIFERA WHOLEGD1Z9GY1FWACTIB

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
3657e2e2-8488-0baf-e063-6394a90a30b317e33680-1767-e957-e063-6394a90a95e22025-05-30WarningsExact identifier
spl set id: 17e33680-1767-e957-e063-6394a90a95e2

Reported adverse events (FAERS/openFDA)#

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