NDC 10096-0121 Skin So Soft Bug Guard Plus Ir3535 Expedition Insect Repellent Sunscreen

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:
10096-0121
Proprietary Name:
Skin So Soft Bug Guard Plus Ir3535 Expedition Insect Repellent Sunscreen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
New Avon Llc
Labeler Code:
10096
Start Marketing Date: [9]
02-12-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-0121-1

Package Description: 118 mL in 1 BOTTLE, SPRAY

NDC Code 10096-0121-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Code 10096-0121-3

Package Description: 236 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 10096-0121?

The NDC code 10096-0121 is assigned by the FDA to the product Skin So Soft Bug Guard Plus Ir3535 Expedition Insect Repellent Sunscreen which is product labeled by New Avon Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 10096-0121-1 118 ml in 1 bottle, spray , 10096-0121-2 59 ml in 1 bottle, spray , 10096-0121-3 236 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 Skin So Soft Bug Guard Plus Ir3535 Expedition Insect Repellent Sunscreen?

Helps prevent sunburn.

Which are Skin So Soft Bug Guard Plus Ir3535 Expedition Insect Repellent Sunscreen UNII Codes?

The UNII codes for the active 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".