NDC 61047-814 Banana Boat Sport Performance
NDC Product Code 61047-814
Proprietary Name: Banana Boat Sport Performance 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: 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
- 61047 - Kik Custom Products
- 61047-814 - Banana Boat Sport Performance
NDC 61047-814-75
Package Description: 88 mL in 1 TUBE
NDC Product Information
Banana Boat Sport Performance with NDC 61047-814 is a product labeled by Kik Custom Products. The generic name of Banana Boat Sport Performance is . The product's dosage form is and is administered via form.
Labeler Name: Kik Custom Products
Dosage Form: -
Product Type: 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.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Kik Custom Products
Labeler Code: 61047
Start Marketing Date: 03-22-2010 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: 12-31-2018 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: I 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’.
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Banana Boat Sport Performance Product Label Images
Banana Boat Sport Performance 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
Drug Facts:Avobenzone: 1%Homosalate: 10%Octisalate: 5%Octicrylene: 0.8%Oxybenzone: 4%Purpose: Sunscreen
Warnings
FOR EXTERNAL USE ONLY.WHEN USING THIS PRODUCT, DO NOT GET INTO EYES IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.STOP USE AND ASK DOCTOR IF IRRITATION OR RASH DEVELOPS. KEEP OUT OF REACH OF CHILDREN.IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.
Inactive Ingredient
Water, Cetearyl Alcohol, Glycerin, Capryly Glycol, Hydrogenated Dimer Dilnoleyl/Dimethyl Carbonate,Copolymer, Cetyl Alcohol, Triethanolamine, Behenyl Acohol, Glyceryl Stearate, Glyceryl Stearate, Citrate,Disodium Ethylene, Dicocamide PEG-15 Disulfate, Sodium Lauroyl Sarcosinate, Carbomer, Xanthan Gum, Aloe Barbadensis Leaf Juice, Retinyl Palmitate (Vitamin A), Tocopherol, Tocopheryl Acetate (Vitamin E), Cetearyl Alchol, Sodium Lauroyl, Lactylate, Lecithin, BHT, Methyl Dibromo Glutaronitrile, Methyl Chloisothiazolinone.Methyl Isothiazolinone, Phenoxy Ethanol, Dipropylene Glycol, Disodium EDTA
Otc - Questions
Questions or Comments: Call 1-800-SAFESUN Mon-Fri.
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