NDC 17630-2002 Banana Boat Kids Tear Free Sunscreen Spf 60

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17630-2002
Proprietary Name:
Banana Boat Kids Tear Free Sunscreen Spf 60
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Accra-pac, Inc.
Labeler Code:
17630
Start Marketing Date: [9]
10-22-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 17630-2002-1

Package Description: 180 mL in 1 CAN

Product Details

What is NDC 17630-2002?

The NDC code 17630-2002 is assigned by the FDA to the product Banana Boat Kids Tear Free Sunscreen Spf 60 which is product labeled by Accra-pac, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 17630-2002-1 180 ml in 1 can . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Banana Boat Kids Tear Free Sunscreen Spf 60?

Apply liberally 15 to 30 minutes before sun exposure. Do not spray directly into face. Spray on hands to apply to face. Rub into skin. Reapply as needed or after swimming, towel drying, perspiring heavily, washing or vigorous activity.

Which are Banana Boat Kids Tear Free Sunscreen Spf 60 UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Banana Boat Kids Tear Free Sunscreen Spf 60 Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".