ASCOPHYLLUM NODOSUM
UNII 168S4EO8YJ

Substance Identification & Data

This profile provides standardized clinical and technical data for Ascophyllum Nodosum, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 168S4EO8YJ.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 84775-78-0 and the RxNorm Concept ID (RxCUI) 1311127. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
168S4EO8YJ
CAS Registry Number
84775-78-0
RxNorm Concept ID
1311127

Detailed Substance Profile

Preferred Name
ASCOPHYLLUM NODOSUM
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
168S4EO8YJ
The specific atomic composition represented as a molecular structure string.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
11331
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
52969
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 Ascophyllum Nodosum. 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

ASCOPHYLLUM NODOSUM
ASCOPHYLLUM NODOSUM EXTRACT
ASCOPHYLLUM NODOSUM POWDER

Common Names & Synonyms

ASCOPHYLLUM NODOSUM [WHO-DD]
ASCOPHYLLUM NODOSUM WHOLE
EGG WRACK
KNOTTED KELP
KNOTTED WRACK
KNUPPETANG
NORWEGIAN KELP
ROCKWEED
ROCKWEED [HOC]

Systematic Nomenclature

ASCOPHYLLUM NODOSUM (LINNAEUS) LE JOLIS 1863

NDC Products Containing ASCOPHYLLUM NODOSUM

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

Manufacturer Quick Index

→ 9055-7588 Quebec Inc. DBA Attitude 7
→ Alberto-Culver USA Inc. 1
→ Bentley Laboratories, LLC 1
→ BioChemics, Inc. 4
→ CLINIQUE LABORATORIES INC 1
→ CONOPCO Inc. d/b/a Unilever 2
→ Caball Sales, Inc. 1
→ Colorescience 1
→ Cosmetic Laboratories of America 1
→ Guna spa 1
→ H2O PLUS 1
→ June Jacobs Labs, LLC 1
→ Jurlique International 1
→ LANGE SAS 2
→ Laboratoire Dr. Renaud 1
→ Lange SAS 1
→ Laura Mercier Cosmetics 14
→ Laura Mercier US Buyer LLC 14
→ Nippon Shikizai, Inc. 1
→ Pacifica Beauty, LLC 1
→ Topiderm, Inc. 2

9055-7588 Quebec Inc. DBA Attitude

Alberto-Culver USA Inc.

Bentley Laboratories, LLC

NDC Product

Waterbright Radiating
NDC 54111-129

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

BioChemics, Inc.

NDC Product

Bio-scriptives Repiderm
NDC 60608-012

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

Bio-scriptives Extreme Af
NDC 60608-013

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

Bio-scriptives Extreme Af
NDC 60608-013

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

Bio-scriptives Extreme Pr
NDC 60608-013

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

CLINIQUE LABORATORIES INC

CONOPCO Inc. d/b/a Unilever

NDC Product

St. Ives Green Tea Cleanser
NDC 64942-1246

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

St. Ives Green Tea Scrub
NDC 64942-1247

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

Caball Sales, Inc.

NDC Product
Human Otc Drug

Dzul Anti-dandruff Conditioner
NDC 83037-002

Generic Name
Pyrithione Zinc
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Colorescience

Cosmetic Laboratories of America

Guna spa

NDC Product
Human Otc Drug

Anti Age Skin
NDC 17089-046

Generic Name
Alpha-tocopherol - Ascophyllum Nodosum - Botryoglossum Platy...
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

H2O PLUS

June Jacobs Labs, LLC

Jurlique International

LANGE SAS

NDC Product

Lightening Night Cream
NDC 51830-020

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

Dark Spot Corrector
NDC 51830-023

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

Laboratoire Dr. Renaud

NDC Product

Sebobalance Spot Control
NDC 62499-384

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

Lange SAS

NDC Product

Lightening Serum
NDC 51830-022

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

Laura Mercier Cosmetics

Laura Mercier US Buyer LLC

Nippon Shikizai, Inc.

NDC Product
Human Otc Drug

Noevir Raysela Uv Shield Primer
NDC 24509-0001

Generic Name
Zinc Oxide, Octinoxate
Dosage Form
Cream
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
Active Listing

Pacifica Beauty, LLC

NDC Product
Human Otc Drug

Glow Baby Brightening Setting Mist Spf 45
NDC 61197-205

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

Topiderm, Inc.

NDC Product
Human Otc Drug

Age Defense For Eyes 5 In 1
NDC 51326-126

Generic Name
Zinc Oxide And Titanium Dioxide
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record