NDC 84509-048 Aoao Retinol Anti-aging Serum

Collagen, Butyrospermum Parkii (shea) Butter Extract, Hyaluronic Acid, Caffeine, - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

Get all the details for National Drug Code (NDC) 84509-048 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
84509-048
Proprietary Name:
Aoao Retinol Anti-aging Serum
Non-Proprietary Name: [1]
Collagen, Butyrospermum Parkii (shea) Butter Extract, Hyaluronic Acid, Caffeine, Simmondsia Chinensis (jojoba) Seed Oil, Retinol
Substance Name: [2]
Butyrospermum Parkii (shea) Butter Extract; Caffeine; Collagen, Soluble, Fish Skin; Hyaluronic Acid; Retinol; Simmondsia Chinensis (jojoba) Seed Oil
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Labeler Code:
84509
FDA Application Number: [6]
M016
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
11-08-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
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Product Details

What is NDC 84509-048?

The NDC code 84509-048 is assigned by the FDA to the product Aoao Retinol Anti-aging Serum which is a human over the counter drug product labeled by Guangdong Junhui Biotechnology Co., Ltd. The generic name of Aoao Retinol Anti-aging Serum is collagen, butyrospermum parkii (shea) butter extract, hyaluronic acid, caffeine, simmondsia chinensis (jojoba) seed oil, retinol. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 84509-048-01 50 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Aoao Retinol Anti-aging Serum?

This product is used as Anti-wrinkle Nourish Moisturizing Firming Anti-aging . 1. After cleansing, use a dropper to drop 3-5 drops of essence on the palm of your hand (applicable before or after toner) 2. Apply evenly on the face and neck, and gently massage until fully moisturized 3. The essence does not need to be washed off, and subsequent skin care steps can be performed after it is fully absorbed

What are Aoao Retinol Anti-aging Serum Active Ingredients?

An 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.
  • BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT 2000 mg/50mL
  • CAFFEINE 500 mg/50mL - A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling.
  • COLLAGEN, SOLUBLE, FISH SKIN 2500 mg/50mL
  • HYALURONIC ACID 2500 mg/50mL - A natural high-viscosity mucopolysaccharide with alternating beta (1-3) glucuronide and beta (1-4) glucosaminidic bonds. It is found in the UMBILICAL CORD, in VITREOUS BODY and in SYNOVIAL FLUID. A high urinary level is found in PROGERIA.
  • RETINOL 450 mg/50mL
  • SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL 500 mg/50mL

Which are Aoao Retinol Anti-aging Serum UNII Codes?

The UNII codes for the active ingredients in this product are:

  • RETINOL (UNII: G2SH0XKK91)
  • RETINOL (UNII: G2SH0XKK91) (Active Moiety)
  • HYALURONIC ACID (UNII: S270N0TRQY)
  • HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
  • CAFFEINE (UNII: 3G6A5W338E)
  • CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
  • COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W)
  • COLLAGEN, SOLUBLE, FISH SKIN (UNII: 8JC99XGU4W) (Active Moiety)
  • SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
  • SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M) (Active Moiety)
  • BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT (UNII: K49155WL9Y)
  • BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT (UNII: K49155WL9Y) (Active Moiety)

Which are Aoao Retinol Anti-aging Serum Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for Aoao Retinol Anti-aging Serum?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An 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.

[3] What kind of product is this? - Indicates 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This 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.

[8] What is the Marketing Category? - Product 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".