NDC 49893-100 Total Suncare Sunscreen Spf 15

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:
49893-100
Proprietary Name:
Total Suncare Sunscreen Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Total Suncare Llc
Labeler Code:
49893
Start Marketing Date: [9]
11-25-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49893-100-01

Package Description: 177 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 49893-100?

The NDC code 49893-100 is assigned by the FDA to the product Total Suncare Sunscreen Spf 15 which is product labeled by Total Suncare Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49893-100-01 177 ml in 1 bottle, spray . 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 Total Suncare Sunscreen Spf 15?

Uses- Helps prevent sunburn   - Higher SPF gives more sunburn protection  - Provides moderate protection against sunburn- Retains SPF after 40 minutes of activity in the water Directions- Apply evenly before sun exposure and as needed.- Hold can about 6in away from body and spray onto skin.- Do not spray onto face - spray into palm and smooth over face and neck.- Children under 6 months of age: ask a doctor.- Reapply as needed or after towel drying, swimming, or perspiring.

Which are Total Suncare Sunscreen Spf 15 UNII Codes?

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

Which are Total Suncare Sunscreen Spf 15 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:

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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".