NDC 63354-789 Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50

Titanium Dioxide, Zinc Oxide

NDC Product Code 63354-789

NDC CODE: 63354-789

Proprietary Name: Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 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: Titanium Dioxide, Zinc Oxide 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

  • 63354 - Edgewell Personal Care Brands Llc
    • 63354-789 - Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50

NDC 63354-789-33

Package Description: 142 g in 1 CAN

NDC 63354-789-36

Package Description: 220 g in 1 CAN

NDC Product Information

Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 with NDC 63354-789 is a a human over the counter drug product labeled by Edgewell Personal Care Brands Llc. The generic name of Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 is titanium dioxide, zinc oxide. The product's dosage form is aerosol, spray and is administered via topical form.

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

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.

Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 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.

  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • BANANA (UNII: 4AJZ4765R9)
  • POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • LEVOMENOL (UNII: 24WE03BX2T)
  • SODIUM GLUCONATE (UNII: R6Q3791S76)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
  • WATER (UNII: 059QF0KO0R)
  • BENTONITE (UNII: A3N5ZCN45C)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • OCTADECANE (UNII: N102P6HAIU)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • ISOCETYL STEAROYL STEARATE (UNII: IJV4LS383R)
  • METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

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: Edgewell Personal Care Brands Llc
Labeler Code: 63354
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: 10-01-2021 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: 12-31-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 Product Label Images

Banana Boat Kids Mineral 100% Mineral Based Sunscreen Uva/uvb Broad Spectrum Spf 50 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 Ingredients

TITANIUM DIOXIDE 3.4%, ZINC OXIDE 16.0%

Purpose

Sunscreen

Uses

  • Helps prevent sunburnif used as directed with other sun protection measures (see
  • Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

​For external use onlyMay stain some fabrics.Contents under pressure. Do not puncture or incinerate container. Do not expose to heat or store at temperatures above 120°F.
Flammable: Do not use in the presence of a flame or spark. Keep away from sources of ignition - No smoking

Do Not Use

On damaged or broken skin.

When Using This Product

• Keep away from face to avoid breathing it • keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor

If rash occurs.

Keep Out Of Reach Of Children.

If product is swallowed, get medical help or contact a Poison Control Center right away

Directions

• Hold container 4 to 6 inches from the skin to apply • Spray liberally and spread evenly by hand 15 minutes before sun exposure •
Do not spray directly into face. Spray on hands and then apply to face • Do not apply in windy conditions • Use in a well-ventilated area • Reapply: • after 80 minutes of swimming or sweating • Immediately after towel drying • At least every 2 hours • Children under 6 months: Ask a doctor •
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.–2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses

Inactive Ingredients:

Water, Butyloctyl Salicylate, Isononyl Isononanoate, Dicaprylyl Carbonate, Propanediol, Isocetyl Stearoyl Stearate, Methyl Dihydroabietate, Cetearyl Alcohol, Sodium Stearoyl Glutamate, C18-21 Alkane, Polyester-8, Bentonite, Caprylyl Glycol, Coco-Glucoside, Microcrystalline Cellulose, Tocopherol, Silica, Citric Acid, Polyhydroxystearic Acid, Alumina, Bisabolol, Sodium Gluconate, Caprylhydroxamic Acid, Glycerin, Cellulose Gum, Aloe Barbadensis Leaf Juice, Musa Sapientum (Banana) Fruit Extract.

Other Information:

  • Protect this product from excessive heat and direct sun

* Please review the disclaimer below.