SANGUISORBA OFFICINALIS ROOT
UNII 4NYV2HT01X

Substance Identification & Data

This profile provides standardized clinical and technical data for Sanguisorba Officinalis Root, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 4NYV2HT01X.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number N/A and the RxNorm Concept ID (RxCUI) 1307954. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
4NYV2HT01X
CAS Registry Number
N/A
RxNorm Concept ID
1307954

Detailed Substance Profile

Preferred Name
SANGUISORBA OFFICINALIS ROOT
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
4NYV2HT01X
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
C71790
National Cancer Institute reference terminology for clinical and research data.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
25306
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
137457
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
SAOF3
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
33026
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCSCMP-2902130
Record ID from the Kew Royal Botanic Gardens Medicinal Plants Name Service.

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Sanguisorba Officinalis Root. 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

SANGUISORBA OFFICINALIS ROOT EXTRACT

Common Names & Synonyms

BURNET EXTRACT
BURNET ROOT [MART.]
BURNET-BLOODWORT ROOT
DI YU
DI YU ROOT
DIYU (SANGUISORBA OFFICINALIS)
GARDEN BURNET ROOT (SANGUISORBA OFFICINALIS)
GREAT BURNET ROOT
OFFICIAL BURNET ROOT
POTERIUM OFFICINALE ROOT
SANGUISORBA MICROCEPHALA ROOT
SANGUISORBA OFFICINALIS ROOT
SANGUISORBA OFFICINALIS ROOT [WHO-DD]
SANGUISORBAE RADIX
SANGUISORBAE RADIX (SANGUISORBA OFFICINALIS)
SANGUISORBAE RADIX (SANGUISORBA OFFICINALIS) [CHP]

NDC Products Containing SANGUISORBA OFFICINALIS ROOT

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

Manufacturer Quick Index

→ AHAVA Dead Sea Laboratories Ltd 1
→ Bliss World LLC 2
→ CODENATURE INC 1
→ Cosmecca Korea Co., Ltd. 1
→ Dime Beauty Co, LLC 1
→ H2O Plus 1
→ Kamedis 3
→ L'Oreal USA Products Inc 3
→ MADISON ONE ACME INC 1
→ Malin and Goetz Inc 1
→ Natural Technology, LLC 1
→ ORIGINS NATURAL RESOURCES INC. 1
→ Professional Complementary Health Formulas 1
→ SHISEIDO AMERICAS CORPORATION 35
→ SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS 2
→ Shenzhen Ishan Technology Co., Ltd 1
→ Shiseido Americas Corporation 2
→ SugarEn Co., Ltd. 1
→ Swiss-American CDMO, LLC 1

AHAVA Dead Sea Laboratories Ltd

Bliss World LLC

CODENATURE INC

Cosmecca Korea Co., Ltd.

NDC Product

Always Perfect Cc
NDC 53727-105

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

Dime Beauty Co, LLC

NDC Product
Human Otc Drug

Creamy Foam Cleanser
NDC 82870-002

Generic Name
Salicylic Acid
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

H2O Plus

Kamedis

NDC Product
Human Otc Drug

Calm Eczema Therapy Cream
NDC 50718-0011

Generic Name
Sulphur 12x
Dosage Form
Cream
Route
Topical
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Clear Acne Spot Treatment
NDC 50718-0032

Generic Name
Acne Spot Treatment
Dosage Form
Liquid
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product

Clear Acne Kit
NDC 50718-0034

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

L'Oreal USA Products Inc

MADISON ONE ACME INC

NDC Product
Human Otc Drug

Fargelin Hemorrhoidal
NDC 55614-610

Generic Name
Calamine, Petrolatum And Phenylephrine Hydrochloride
Dosage Form
Ointment
Route
Rectal; Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Malin and Goetz Inc

NDC Product

Acne Treatment Daytime
NDC 53634-125

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

Natural Technology, LLC

ORIGINS NATURAL RESOURCES INC.

Professional Complementary Health Formulas

NDC Product
Human Otc Drug

Large Intestine Formula 2103
NDC 63083-2103

Generic Name
Large Intestine Formula
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

SHISEIDO AMERICAS CORPORATION

NDC Product
Human Otc Drug

Shiseido Essential Energy Hydrating Day
NDC 58411-656

Generic Name
Homosalate, Octocrylene, Octisalate, And Avobenzone
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Shiseido Revitalessence Skin Glow Primer
NDC 58411-894

Generic Name
Avobenzone, Octinoxate, And Octocrylene
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS

NDC Product

Spai-sons Marigold Oily Skin
NDC 66854-023

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

Feix Facial
NDC 66854-024

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

Shenzhen Ishan Technology Co., Ltd

NDC Product
Human Otc Drug

Ishancare
NDC 73076-178

Generic Name
First Aid Burn Ointment
Dosage Form
Ointment
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Shiseido Americas Corporation

NDC Product
Human Otc Drug

Shiseido Urban Environment
NDC 58411-952

Generic Name
Ensulizole, Homosalate, Octisalate, Zinc Oxide
Dosage Form
Emulsion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

SugarEn Co., Ltd.

NDC Product

Rgo Nutriment Rich Mask
NDC 81897-505

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

Swiss-American CDMO, LLC

External Clinical & Regulatory Resources

NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record
NIH
NCI Thesaurus