NDC 61924-410 Renew Dimethicone Skin Protectant

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:
61924-410
Proprietary Name:
Renew Dimethicone Skin Protectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermarite Industries Llc
Labeler Code:
61924
Start Marketing Date: [9]
03-15-2012
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 61924-410-04

Package Description: 113 g in 1 TUBE

NDC Code 61924-410-05

Package Description: 5 g in 1 PACKET

Product Details

What is NDC 61924-410?

The NDC code 61924-410 is assigned by the FDA to the product Renew Dimethicone Skin Protectant which is product labeled by Dermarite Industries Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61924-410-04 113 g in 1 tube , 61924-410-05 5 g in 1 packet . 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 Renew Dimethicone Skin Protectant?

Clean skin gently with mild skin cleanser. Pat dry or allow to air dry. Apply as necessary. If applying to perineal area, apply after each incontinent episode or diaper change to promote comfort and long lasting protection.

Which are Renew Dimethicone Skin Protectant UNII Codes?

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

Which are Renew Dimethicone Skin Protectant 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".