NDC 73206-020 Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30

Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30

NDC Product Code 73206-020

NDC Code: 73206-020

Proprietary Name: Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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: Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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

  • 73206 - Arjolo, Inc.
    • 73206-020 - Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30

NDC 73206-020-01

Package Description: 1 PACKET in 1 PACKAGE > 5.275 g in 1 PACKET

NDC Product Information

Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 with NDC 73206-020 is a a human over the counter drug product labeled by Arjolo, Inc.. The generic name of Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 is bravo sierra usa face sunscreen broad spectrum spf 30. The product's dosage form is swab and is administered via topical form.

Labeler Name: Arjolo, Inc.

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.

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.

Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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.


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.

Product Labeler Information

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

Labeler Name: Arjolo, Inc.
Labeler Code: 73206
FDA Application Number: part333A 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: 07-11-2019 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.

Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 Product Label Images

Bravo Sierra Usa Face Sunscreen Broad Spectrum Spf 30 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

Benzalkonium Chloride 0.1%




• To decrease bacteria on the skin.


For external use onlyWhen using this product do not use in or near eyes. If contact occurs, flush thoroghly with water.

Stop use if irritation or redness developes. If condition persists for more than 72 hours, contact a doctor.

Keep Out Of Reach Of Children

Unless under adult supervision. If swallowed get medical help or contact a poison control center right away


• tear open packet, remove wipe.• wipe skin thorohly with product and allow to air dry.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Aphanimmanon Flos-Aquaa Extract, Betaine, Citric Acud, Glycerin, Fragrance, Panax Ginseng Root Extract, Polyglyceryl-4 Caprate, Polyglyceryl-4 Cocoate, Polyglyceryl-6 Caprylate,Polyglyceryl-6 Ricinoleate, Sodium Citrate, Water.

* Please review the disclaimer below.

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