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NDC 84509-025 Aoao Snow Bieach Intensive For Face And Body

Ascorbic Acid, Niacinamide, Chamomilla Recutita (matricaria) Extract, Collagen, Milk, - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 84509-025?
  4. Aoao Snow Bieach Intensive For Face And Body Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 84509-025 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:
84509-025
Proprietary Name:
Aoao Snow Bieach Intensive For Face And Body
Non-Proprietary Name: [1]
Ascorbic Acid, Niacinamide, Chamomilla Recutita (matricaria) Extract, Collagen, Milk, Allantoin.
Substance Name: [2]
Allantoin; Ascorbic Acid; Collagen, Soluble, Fish Skin; Cow Milk; Matricaria Chamomilla Whole; Niacinamide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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 Name: [5]
Guangdong Junhui Biotechnology Co., Ltd
Labeler Code:
84509
Product Label ID:
24bc655b-a413-4c2c-e063-6394a90a2d6f
FDA Application Number: [6]
M016
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
10-18-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

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Product Details

What is NDC 84509-025?

The NDC code 84509-025 is assigned by the FDA to the product Aoao Snow Bieach Intensive For Face And Body which is a human over the counter drug product labeled by Guangdong Junhui Biotechnology Co., Ltd. The generic name of Aoao Snow Bieach Intensive For Face And Body is ascorbic acid, niacinamide, chamomilla recutita (matricaria) extract, collagen, milk, allantoin.. The product's dosage form is cream and is administered via topical form. The product is distributed in a single package with assigned NDC code 84509-025-01 50 g 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 Snow Bieach Intensive For Face And Body?

This product is used as Whitening Anti-wrinkle Moisturizing Nourishing Anti-aging . 1 .Clean and dry your skin. 2 . Apply a proper amount of the cream on desired area with your fingers, using a circular motion to massage the cream into the skin. 3 .Please apply it twice a day(morning and evening)

What are Aoao Snow Bieach Intensive For Face And Body 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.
  • ALLANTOIN 500 mg/50g - A urea hydantoin that is found in URINE and PLANTS and is used in dermatological preparations.
  • ASCORBIC ACID 3500 mg/50g - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • COLLAGEN, SOLUBLE, FISH SKIN 900 mg/50g
  • COW MILK 750 mg/50g - The off-white liquid secreted by the mammary glands of humans and other mammals. It contains proteins, sugar, lipids, vitamins, and minerals.
  • MATRICARIA CHAMOMILLA WHOLE 1000 mg/50g
  • NIACINAMIDE 1500 mg/50g - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.

Which are Aoao Snow Bieach Intensive For Face And Body UNII Codes?

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

Which are Aoao Snow Bieach Intensive For Face And Body 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 Snow Bieach Intensive For Face And Body?

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".