NDC 71380-0014 Brucke A.c.c. Calming Cool Suncream

Ethylhexyl Methoxycinnamate, Titanium Dioxide

NDC Product Code 71380-0014

NDC CODE: 71380-0014

Proprietary Name: Brucke A.c.c. Calming Cool Suncream 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: Ethylhexyl Methoxycinnamate, Titanium Dioxide 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

  • 71380 - Nature4 Co., Ltd.
    • 71380-0014 - Brucke A.c.c. Calming Cool Suncream

NDC 71380-0014-1

Package Description: 50 mL in 1 TUBE

NDC Product Information

Brucke A.c.c. Calming Cool Suncream with NDC 71380-0014 is a a human over the counter drug product labeled by Nature4 Co., Ltd.. The generic name of Brucke A.c.c. Calming Cool Suncream is ethylhexyl methoxycinnamate, titanium dioxide. The product's dosage form is cream and is administered via topical form.

Labeler Name: Nature4 Co., Ltd.

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.

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.

Brucke A.c.c. Calming Cool Suncream 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.

  • TITANIUM DIOXIDE 2.6736 g/100mL
  • OCTINOXATE 7.2 g/100mL

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.

  • WATER (UNII: 059QF0KO0R)

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: Nature4 Co., Ltd.
Labeler Code: 71380
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: 12-03-2019 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: 12-31-2020 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.

Brucke A.c.c. Calming Cool Suncream Product Label Images

Brucke A.c.c. Calming Cool Suncream 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

Otc - Active Ingredient

Ethylhexyl Methoxycinnamate(Octinoxate), Titanium Dioxide

Inactive Ingredient

Water, 1,2-Hexanediol, etc

Otc - Purpose

Helps prevent sunburn.

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Apply a sufficient amount to cover the exposed area thoroughly.


1. In case of having side effects such as red rash, swollenness and/or itching while using this cosmetic, or in case such symptoms appear by direct sunlight after using it, consult a dermatologist immediately.

2. Do not apply on skin where there is wound, eczema, or irritation.

3. Storage and cautions for handling.

A) Keep out of reach of children.

B) Avoid the place where the direct sunlight is.

4. If the cream put on your cloth, do not wash and dry cleaning.

Dosage & Administration

For external use only

* Please review the disclaimer below.