NDC 63148-225 Instant Hand Sanitizer With Moisturizers And Vitamin E

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:
63148-225
Proprietary Name:
Instant Hand Sanitizer With Moisturizers And Vitamin E
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apollo Health And Beauty Care
Labeler Code:
63148
Start Marketing Date: [9]
07-05-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63148-225-15

Package Description: 443 mL in 1 BOTTLE, PUMP

NDC Code 63148-225-40

Package Description: 1180 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 63148-225?

The NDC code 63148-225 is assigned by the FDA to the product Instant Hand Sanitizer With Moisturizers And Vitamin E which is product labeled by Apollo Health And Beauty Care. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63148-225-15 443 ml in 1 bottle, pump , 63148-225-40 1180 ml in 1 bottle, pump . 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 Instant Hand Sanitizer With Moisturizers And Vitamin E?

USES: TO HELP REDUCE BACTERIA ON THE SKIN.DIRECTIONS: APPLY A SMALL AMOUNT IN YOUR PALM AND RUB HANDS TOGETHER BRISKLY UNTIL DRY. CHILDREN UNDER 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

Which are Instant Hand Sanitizer With Moisturizers And Vitamin E UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Instant Hand Sanitizer With Moisturizers And Vitamin E?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".