LAMINARIA JAPONICA
UNII WE98HW412B

Substance Identification & Data

This profile provides standardized clinical and technical data for Laminaria Japonica, uniquely identified by the FDA Unique Ingredient Identifier (UNII) WE98HW412B.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number N/A and the RxNorm Concept ID (RxCUI) 1426558. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
WE98HW412B
CAS Registry Number
N/A
RxNorm Concept ID
1426558

Detailed Substance Profile

Preferred Name
LAMINARIA JAPONICA
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
WE98HW412B
The specific atomic composition represented as a molecular structure string.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
NCBI Taxonomy
88149
Unique numeric identifier used to specify biological species in the NCBI database.

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Laminaria Japonica. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

FDA Official Name

LAMINARIA JAPONICA EXTRACT

Common Names & Synonyms

CHA-KOMBU
ECKLONIAE THALLUS (LAMINARIA JAPONICA)
JAPANESE KELP
JAPANESE SEA TANGLE
KELP OR TANGLE (LAMINARIA JAPONICA)
KOMBU
KOMBU [HOC]
KUN BU (LAMINARIA JAPONICA)
KUNBU (LAMINARIA JAPONICA)
LAMINARIA FRAGILIS
LAMINARIA JAPONICA
LAMINARIA JAPONICA [WHO-DD]
LAMINARIA JAPONICA WHOLE
LAMINARIAE THALLUS (LAMINARIA JAPONICA)
LAMINARIAE THALLUS (LAMINARIA JAPONICA) [CHP]
SACCHARINA JAPONICA

NDC Products Containing LAMINARIA JAPONICA

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:

Manufacturer Quick Index

→ ABLE C&C CO., LTD. 1
→ Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals 2
→ Almay, Inc. 3
→ Bekeikorea 1
→ CLERIAN, INC. 2
→ Daisy Collection 1
→ ECOMINE Co., Ltd. 4
→ Ecomine Co., Ltd. 1
→ GPNY CORP 1
→ Guangzhou Houkea Biotechnology Co., Ltd. 2
→ Jeun Cell Ltd 2
→ LG H&H CO., LTD. 5
→ MONOGLOT HOLDINGS Inc. 2
→ MY Corp.,Ltd 1
→ Memebox Corporation 1
→ Mi-face Co., Ltd 2
→ Professional Complementary Health Formulas 2
→ Revamp International Pte. Ltd. 3
→ S-ONE PHARMACEUTICAL INC 2
→ SEORIN COMPANY Co., Ltd. 2
→ SY Global Inc 2
→ TIMEBIO Co., Ltd 2
→ Tonymoly Co., Ltd. 2
→ VS Shinbi Co., Ltd. 3
→ YENSA Beauty, LLC 16

ABLE C&C CO., LTD.

Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals

NDC Product
Human Otc Drug

Jba Joint Revive Tm The Legend Caffe Latte
NDC 13411-858

Generic Name
Glucosamine Sulfate Potassium Chloride,chondroitin Sulfate,f...
Dosage Form
Powder
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Otc Drug

Jba Joint Revive The Legend I
NDC 13411-859

Generic Name
Glucosamine Sulfate Potassium Chloride,fucoidan Extract,eggs...
Dosage Form
Capsule
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Almay, Inc.

Bekeikorea

CLERIAN, INC.

NDC Product

Clerian H
NDC 69767-102

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Clerian
NDC 69767-103

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

Daisy Collection

NDC Product

Daisy Care Wipes
NDC 77748-201

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

ECOMINE Co., Ltd.

NDC Product

Hasol Intensive Scalp Tonic
NDC 51270-120

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Hasol Anagen Hair Tonic
NDC 51270-122

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Hasol Anagen Scalp
NDC 51270-123

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Hasol Anti Hair Loss
NDC 51270-124

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

Ecomine Co., Ltd.

NDC Product

Hasol Intensive
NDC 51270-119

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH FINAL
Inactive / Discontinued

GPNY CORP

NDC Product
Human Otc Drug

Jmsolution Marine Luminous Pearl Sunscreen
NDC 84754-052

Generic Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Guangzhou Houkea Biotechnology Co., Ltd.

Jeun Cell Ltd

LG H&H CO., LTD.

NDC Product
Human Otc Drug

Belif Aqua Bomb - Glow Sunstick Spf50
NDC 53208-730

Generic Name
Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methox...
Dosage Form
Stick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Belif Aqua Bomb - Glow Sunstick Spf50
NDC 53208-731

Generic Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage Form
Stick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

MONOGLOT HOLDINGS Inc.

NDC Product
Human Otc Drug

Elroel Pang Pang Sun Cushion S7
NDC 83154-003

Generic Name
Zinc Oxide, Titanium Dioxide, Octinoxate, Octisalate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Elroel Pang Pang Sun Cushion Plus
NDC 83154-004

Generic Name
Zinc Oxide, Titanium Dioxide, Octinoxate, Octisalate
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

MY Corp.,Ltd

Memebox Corporation

Mi-face Co., Ltd

NDC Product

Bonange Hand Cleaner
NDC 75005-020

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Bonange Hand Cleaner
NDC 75005-030

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Professional Complementary Health Formulas

NDC Product
Human Otc Drug

Lung Formula 2104
NDC 63083-2104

Generic Name
Lung Formula
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Oxy Bee Pollen Liquescence 3012
NDC 63083-3012

Generic Name
Oxy Bee Pollen Liquescence
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Revamp International Pte. Ltd.

S-ONE PHARMACEUTICAL INC

NDC Product

Moduga Camellia Hair Bar
NDC 74721-0070

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Moduga Woody Hair Bar
NDC 74721-0080

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

SEORIN COMPANY Co., Ltd.

SY Global Inc

NDC Product

Pine Antibacterial Wet Wipes
NDC 77200-002

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

TIMEBIO Co., Ltd

NDC Product

Ato Standard Intensivecream
NDC 81160-202

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

Tonymoly Co., Ltd.

VS Shinbi Co., Ltd.

NDC Product

U-max Wrinkle Serum
NDC 50795-1001

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

U-max Multi Bb
NDC 50795-2001

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

YENSA Beauty, LLC

External Clinical & Regulatory Resources

NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record