NDC 54860-394 Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml

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:
54860-394
Proprietary Name:
Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Lantern Scicence Co Ltd
Labeler Code:
54860
Start Marketing Date: [9]
04-18-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - TRANSPARANT)

Product Packages

NDC Code 54860-394-01

Package Description: 236 mL in 1 TUBE

Product Details

What is NDC 54860-394?

The NDC code 54860-394 is assigned by the FDA to the product Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml which is product labeled by Shenzhen Lantern Scicence Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54860-394-01 236 ml in 1 tube . 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 Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml?

Wet hands thoroughly with product and rub until dry without wipingFor children under 6, use only under adult supervision.Not recommended for infants.

Which are Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml UNII Codes?

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

Which are Mellow Instant Hand Sanitizer With Aloe And Vitamin E 236ml 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".