NDC 73676-010 Abib Quick Sunstick Protection Bar

Octinoxate, Octisalate, Octocrylene

NDC Product Code 73676-010

NDC CODE: 73676-010

Proprietary Name: Abib Quick Sunstick Protection Bar What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Octinoxate, Octisalate, Octocrylene 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.

NDC Code Structure

  • 73676 - Fourcompany Co., Ltd.
    • 73676-010 - Abib Quick Sunstick Protection Bar

NDC 73676-010-02

Package Description: 1 CONTAINER in 1 CARTON > 22 g in 1 CONTAINER (73676-010-01)

NDC Product Information

Abib Quick Sunstick Protection Bar with NDC 73676-010 is a a human over the counter drug product labeled by Fourcompany Co., Ltd.. The generic name of Abib Quick Sunstick Protection Bar is octinoxate, octisalate, octocrylene. The product's dosage form is stick and is administered via topical form.

Labeler Name: Fourcompany Co., Ltd.

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

Product Type: Human Otc Drug 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.

Abib Quick Sunstick Protection Bar Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • OCTINOXATE 1.54 g/22g
  • OCTISALATE .99 g/22g
  • OCTOCRYLENE .44 g/22g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Fourcompany Co., Ltd.
Labeler Code: 73676
FDA Application Number: part352 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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.

Start Marketing Date: 02-01-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Abib Quick Sunstick Protection Bar Product Label Images

Abib Quick Sunstick Protection Bar Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Active Ingredient:Ethylhexyl Methoxycinnamate 7.0%Ethylhexyl Salicylate 4.5%Octocrylene 2.0%

Inactive Ingredient

Inactive Ingredients:Octyldodecanol, Butylene Glycol Dicaprylate/Dicaprate, Dibutyl Ethylhexanoyl Glutamide, Dibutyl Lauroyl Glutamide, Diisostearyl Malate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Dextrin Palmitate, Water, Butylene Glycol, Saccharide Isomerate, Glycerin, Maltodextrin, Hydrolyzed Vegetable Protein, Caprylic/Capric Triglyceride, Camellia Sinensis Leaf Extract, Hydrogenated Lecithin, Phenoxyethanol, Ethyl Hexanediol, Centella Asiatica Extract, Ceramide NP, Aloe Barbadensis Leaf Juice, Citric Acid, Sodium Citrate, Cucumis Sativus (Cucumber) Fruit Extract, Aloe Barbadensis Leaf Extract, Ethylhexylglycerin

Purpose

Purpose: Sunscreen

Warnings

Warnings:1. If there is any abnormal symptom or side effect such as red spot, swelling, or itchiness when or after using the product please consult with a specialist2. Do not use on scarred areas3. Precautions for storage and handling:1) Keep out of reach of children2) Store away from direct sunlight

Description

Direction:■ Slowly twist the dial in the bottom for the content to come out.■ For face, after skincare, directly apply the product onto the skin and lightly pat it to be completely absorbed.■ For body, directly apply the product to any exposed areas to ensure your skin is protected from the sun.Uses: ■ Helps protect skin from excessive exposure to UV rays.■ Moisturizing texture perfectly gets absorbed into the skin without any white cast leaving fresh and softly matt finish.■ Stick formula provides easy and fast application without having to use the hands.

* Please review the disclaimer below.