74458-099 NDC - GZE MASSAGE OIL (PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) SEED OIL 43.45% OLEA EUROPAEA (OLIVE) FRUIT OIL 21.3% SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL 10.3% CITRUS PARADISI (GRAPEFRUIT) PEEL OIL 10% CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL 10% EUCALYPTOL 4.55%)

Drug Information

  • Product NDC: 74458-099
  • Proprietary Name: GZE Massage Oil
  • Non Proprietary Name: Prunus Amygdalus Dulcis (Sweet Almond) Seed Oil 43.45% Olea Europaea (Olive) Fruit Oil 21.3% Simmondsia Chinensis (Jojoba) Seed Oil 10.3% Citrus Paradisi (Grapefruit) Peel Oil 10% Citrus Aurantium Bergamia (Bergamot) Fruit Oil 10% Eucalyptol 4.55%
  • Active Ingredient(s): 10 g/100mL CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL; 10 g/100mL CITRUS PARADISI (GRAPEFRUIT) PEEL OIL; 4.55 g/100mL EUCALYPTOL; 21.3 g/100mL OLEA EUROPAEA (OLIVE) FRUIT OIL; 43.45 g/100mL PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL; 10.3 g/100mL SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
  • Administration Route(s): TOPICAL
  • Dosage Form(s): OIL
  • Pharmacy Class(es): Lipid Emulsion [EPC]; Lipids [CS]

Labeler Information

Field Name Field Value
Labeler Name: Guangzhou Yilong Cosmetics Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: M016
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:7/4/2024

Package Information

No. Package Code Package Description Billing Unit
174458-099-01237 mL in 1 BOTTLE, PUMP (74458-099-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74458-099The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEGZE Massage OilThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPrunus Amygdalus Dulcis (Sweet Almond) Seed Oil 43.45% Olea Europaea (Olive) Fruit Oil 21.3% Simmondsia Chinensis (Jojoba) Seed Oil 10.3% Citrus Paradisi (Grapefruit) Peel Oil 10% Citrus Aurantium Bergamia (Bergamot) Fruit Oil 10% Eucalyptol 4.55%The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEOILThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE7/4/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM016This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGuangzhou Yilong Cosmetics Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL; CITRUS PARADISI (GRAPEFRUIT) PEEL OIL; EUCALYPTOL; OLEA EUROPAEA (OLIVE) FRUIT OIL; PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL; SIMMONDSIA CHINENSIS (JOJOBA) SEED OILAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 10; 4.55; 21.3; 43.45; 10.3 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL 
PHARM CLASSESLipid Emulsion [EPC], Lipids [CS] 

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This page was last updated on: 12/6/2025

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