84509-026 NDC - AOAO RETIOL ANTI-WRINKLE CREAM (COLLAGEN,HYALURONIC ACID,BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT,CAFFEINE,SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL,RETINOL.)

Drug Information

  • Product NDC: 84509-026
  • Proprietary Name: AOAO Retiol Anti-Wrinkle Cream
  • Non Proprietary Name: Collagen,Hyaluronic Acid,Butyrospermum Parkii (Shea) Butter Extract,Caffeine,Simmondsia Chinensis (Jojoba) Seed Oil,Retinol.
  • Active Ingredient(s): 1300 mg/130g CAFFEINE; 6500 mg/130g COLLAGEN, SOLUBLE, FISH SKIN; 6500 mg/130g HYALURONIC ACID; 1300 mg/130g JOJOBA OIL; 1170 mg/130g RETINOL; 5200 mg/130g SHEA BUTTER
  • Administration Route(s): TOPICAL
  • Dosage Form(s): CREAM
  • Pharmacy Class(es): Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]; Methylxanthine [EPC]; Xanthines [CS]

Labeler Information

Field Name Field Value
Labeler Name: Guangdong Junhui Biotechnology Co., LTD
Product Type: HUMAN OTC DRUG
FDA Application Number: M016
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:10/21/2024

Package Information

No. Package Code Package Description Billing Unit
184509-026-01130 g in 1 BOTTLE (84509-026-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC84509-026The 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 NAMEAOAO Retiol Anti-Wrinkle CreamThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECollagen,Hyaluronic Acid,Butyrospermum Parkii (Shea) Butter Extract,Caffeine,Simmondsia Chinensis (Jojoba) Seed Oil,Retinol.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe 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 DATE10/21/2024This 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 NAMEGuangdong Junhui Biotechnology Co., LTDName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECAFFEINE; COLLAGEN, SOLUBLE, FISH SKIN; HYALURONIC ACID; JOJOBA OIL; RETINOL; SHEA BUTTERAn 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 STRENGTH1300; 6500; 6500; 1300; 1170; 5200 
ACTIVE INGRED UNITmg/130g; mg/130g; mg/130g; mg/130g; mg/130g; mg/130g 
PHARM CLASSESCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS] 

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

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