BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES
UNII 0C9AC7D6XU

Substance Identification & Data

This profile provides standardized clinical and technical data for Butyrospermum Parkii (shea) Butter Unsaponifiables, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 0C9AC7D6XU.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 225234-14-0 and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
0C9AC7D6XU
CAS Registry Number
225234-14-0
RxNorm Concept ID
N/A

Detailed Substance Profile

Preferred Name
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
0C9AC7D6XU
The specific atomic composition represented as a molecular structure string.
Substance Type
structurallyDiverse
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
ITIS TSN
505960
Taxonomic Serial Number for species identified in the Integrated Taxonomic Information System.
NCBI Taxonomy
292385
Unique numeric identifier used to specify biological species in the NCBI database.
USDA PLANTS ID
VIPA12
Botanical identifier maintained by the U.S. Department of Agriculture.
GRIN Nomen ID
102598
Identifier from the Germplasm Resources Information Network botanical database.
MPNS Record
WCS-213267
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 Butyrospermum Parkii (shea) Butter Unsaponifiables. 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

BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES

Common Names & Synonyms

BUTYROSPERMUM PARKII BUTTER UNSAPONIFIABLES
FATS AND GLYCERIDIC OILS, SHEA BUTTER, UNSAPONIFIABLE FRACTION
SHEA BUTTER UNSAPONIFIABLES

Brand / Trade Names

KARITE NONSAPONIFIABLE

NDC Products Containing BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES

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

Manufacturer Quick Index

→ Amyris, Inc 1
→ BEL STAR S A 4
→ COOLA LLC 1
→ Canadian Custom Packaging Company 1
→ Cleoslab Co., Ltd 1
→ Dongguan Haiyi Technology Co.,Ltd. 1
→ ENCHANTE ACCESSORIES INC. 21
→ Eden Brands, Inc. 1
→ Epicuren Disocovery 1
→ Farouk Systems, Inc. 2
→ Guangdong Bisutang Biotechnology Co., Ltd. 1
→ Guangdong Youbaijia Cosmetic Industry Co., Ltd 1
→ Guangzhou Kadiya Biotechnology Co., Ltd. 3
→ Guangzhou Yilong Cosmetics Co., Ltd 6
→ Industria La Popular, S.A. 4
→ Intelligent Skin Care Inc. 1
→ Kramer Laboratories 1
→ LCA COSMETICS LLC 2
→ LOTUSA LLC 1
→ LOTUSA LLC. 2
→ Lather, Inc. 1
→ Natural Korea Co., Ltd. 1
→ Oneskin Cosmetics Co., Ltd. 1
→ Peer Pharm Ltd. 1
→ RENU LABORATORIES, INC. 1
→ REVLON 1
→ REVLON CONSUMER PRODUCTS CORP 1
→ Renu Laboratories, Inc. 1
→ Revlon 1
→ SOLARA SUNCARE, INC. 1
→ Shandong Yuyaotang Pharmaceutical Co., Ltd 1
→ Shenzhen Weikemo Intelligent Technology CO.,LTD 1
→ Shenzhen Zhumeng Times Technology Co., Ltd. 11
→ Shield and Heal Inc. 2
→ Sonovio LLC 1
→ Standard Procedure Inc 1
→ Stream2Sea, LLC 1
→ Sunsolve MD Inc 1
→ Supergoop, LLC 5
→ THE WONDERFUL GROUP LLC 1
→ The Avon Company 1
→ The Center Brands, LLC 1
→ The Honest Company, Inc. 1
→ Topiderm, Inc. 1
→ Tubby Todd 1
→ Vacation Inc. 1
→ Xiamen Beishan Ecommerce Co.,LTD 1
→ Zax Healthcare Inc. 1
→ doTERRA International, LLC 1

Amyris, Inc

NDC Product
Human Otc Drug

Pipette Diaper Rash
NDC 73517-427

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

BEL STAR S A

COOLA LLC

Canadian Custom Packaging Company

NDC Product

Zaxs Aches And Pain
NDC 54291-054

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

Cleoslab Co., Ltd

Dongguan Haiyi Technology Co.,Ltd.

NDC Product

Herbal Salve
NDC 84732-918

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

ENCHANTE ACCESSORIES INC.

Eden Brands, Inc.

NDC Product
Human Otc Drug

Evereden Healing Eczema Treatment
NDC 72113-106

Generic Name
Colloidal Oatmeal
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Epicuren Disocovery

NDC Product
Human Otc Drug

Anti Aging Lip Balm Pot Spf 15
NDC 84378-103

Generic Name
Lip Balm
Dosage Form
Ointment
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Farouk Systems, Inc.

NDC Product

Biosilk Gardenia
NDC 73740-5001

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

Biosilk Pomegranite
NDC 73740-5003

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

Guangdong Bisutang Biotechnology Co., Ltd.

Guangdong Youbaijia Cosmetic Industry Co., Ltd

NDC Product

Barubt Night Renewal Cream
NDC 84712-006

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

Guangzhou Kadiya Biotechnology Co., Ltd.

NDC Product

Whitening Exfoliatingsoap
NDC 84423-012

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Inactive / Discontinued
NDC Product
Human Otc Drug

Strongwhiteningsoap
NDC 84423-053

Generic Name
Strongwhiteningsoap
Dosage Form
Soap
Route
Cutaneous
Marketing
OTC MONOGRAPH DRUG
Active Listing

Guangzhou Yilong Cosmetics Co., Ltd

NDC Product

Gze African Blacksoap
NDC 83566-049

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

Gze Hotsoap
NDC 83566-220

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

Gze Stretch Mark Balm
NDC 83566-271

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

Melao Hair Wax Stick
NDC 83566-591

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

Industria La Popular, S.A.

Intelligent Skin Care Inc.

Kramer Laboratories

NDC Product
Human Otc Drug

Nizoral Eczema Relief Cream
NDC 55505-223

Generic Name
Colloidal Oatmeal
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

LCA COSMETICS LLC

LOTUSA LLC

NDC Product

Biorlx Lip Balm Hemp
NDC 80554-001

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

LOTUSA LLC.

NDC Product

Biorlx Lip Balm Collagen
NDC 80554-002

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

Biorlx Lip Balm Ginseng
NDC 80554-003

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

Lather, Inc.

Natural Korea Co., Ltd.

NDC Product

Anti-bacterial Hand Cream
NDC 74646-0017

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

Oneskin Cosmetics Co., Ltd.

NDC Product

Derma Eaude Glatok Cream
NDC 70889-910

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

Peer Pharm Ltd.

NDC Product
Human Otc Drug

Botao Baby Diaper Rash Cream
NDC 69435-1501

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

RENU LABORATORIES, INC.

REVLON

NDC Product
Human Otc Drug

Ceramide Lift And Firm
NDC 10967-666

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

REVLON CONSUMER PRODUCTS CORP

Renu Laboratories, Inc.

NDC Product

Renu Laboratories Drying
NDC 76348-404

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

Revlon

NDC Product
Human Otc Drug

Prevage Anti-aging Eye Cream Spf 15
NDC 10967-685

Generic Name
Octinoxate, Oxybenzone
Dosage Form
Cream
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

SOLARA SUNCARE, INC.

Shandong Yuyaotang Pharmaceutical Co., Ltd

NDC Product

Oheal Tattoo Numbing Cream
NDC 84746-005

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

Shenzhen Weikemo Intelligent Technology CO.,LTD

NDC Product

Dark Spot Corrector
NDC 81940-001

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

Shenzhen Zhumeng Times Technology Co., Ltd.

NDC Product

5%minoxidil Hair Regrowth
NDC 84372-003

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

5%minoxidil Hair Regrowth
NDC 84372-004

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

5%minoxidil Hair Regrowth
NDC 84372-005

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

5%minoxidil Hair Regrowth
NDC 84372-006

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

5%minoxidil Hair Regrowth
NDC 84372-007

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

5%minoxidil Hair Regrowth
NDC 84372-008

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

5%minoxidil Hair Regrowth
NDC 84372-009

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

5%minoxidil Hair Regrowth
NDC 84372-010

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

5%minoxidil Hair Regrowth
NDC 84372-011

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

5%minoxidil Hair Regrowth
NDC 84372-012

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

5%minoxidil Hair Regrowth
NDC 84372-013

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

Shield and Heal Inc.

NDC Product

Shield And Heal Lip Balm
NDC 81470-002

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

Sonovio LLC

NDC Product

Smts Dual Ha Sun Block
NDC 84609-001

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

Standard Procedure Inc

NDC Product
Human Otc Drug

Standard Procedure Lip Balm Spf 50
NDC 84425-105

Generic Name
Zinc Oxide Homosalate Octocrylene
Dosage Form
Stick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Stream2Sea, LLC

NDC Product
Human Otc Drug

Ecostick Sunscreen Spf 35
NDC 69555-035

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

Sunsolve MD Inc

NDC Product
Human Otc Drug

Sunsovle Md Volumize And Restore
NDC 84878-823

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

Supergoop, LLC

NDC Product
Human Otc Drug

Lipshade Spf 30 Hey Yall
NDC 75936-615

Generic Name
Zinc Oxide
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Lipshade Spf 30 High Five
NDC 75936-616

Generic Name
Zinc Oxide
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Lipshade Spf 30 Love You More
NDC 75936-617

Generic Name
Zinc Oxide
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Lipshade Spf 30 Lucky Me
NDC 75936-618

Generic Name
Zinc Oxide
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc Drug

Lipshade Spf 30 Obsessed
NDC 75936-619

Generic Name
Zinc Oxide
Dosage Form
Lipstick
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

THE WONDERFUL GROUP LLC

NDC Product

Day In The Sun Kit
NDC 80782-001

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

The Avon Company

The Center Brands, LLC

The Honest Company, Inc.

NDC Product
Human Otc Drug

Calm And Heal Melting Balm
NDC 69366-505

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

Topiderm, Inc.

NDC Product
Human Otc Drug

Replenix Sheer Spf 50
NDC 51326-858

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

Tubby Todd

NDC Product
Human Otc Drug

Sweet Cheeks Diaper
NDC 73088-301

Generic Name
Zinc Oxide
Dosage Form
Paste
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Vacation Inc.

NDC Product
Human Otc Drug

Vacation Instant Browning
NDC 80641-521

Generic Name
Avobenzone Octisalate Octocrylene
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Xiamen Beishan Ecommerce Co.,LTD

NDC Product

Oheal Tattoo Numbing Cream
NDC 83910-003

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

Zax Healthcare Inc.

NDC Product

Zaxs Aches And Pain
NDC 82186-162

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

doTERRA International, LLC

External Clinical & Regulatory Resources

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