NDC 61047-814 Banana Boat Sport Performance

  1. Labeler Index
  2. Kik Custom Products
  3. NDC: 61047-814 Banana Boat Sport Performance

NDC Product Code 61047-814

NDC 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.

NDC Code Structure

  • 61047 - Kik Custom Products

NDC 61047-814-75

Package Description: 88 mL in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Banana Boat Sport Performance with NDC 61047-814 is a product labeled by Kik Custom Products. The product's dosage form is and is administered via form.

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 - INACTIVATED, the listing data was inactivated by the FDA. 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".

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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.

* Please review the disclaimer below.