NDC 52985-904 Hand Sanitizer

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:
52985-904
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anhui Oasis Disinfection Products Co., Ltd
Labeler Code:
52985
Start Marketing Date: [9]
06-18-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 52985-904-01

Package Description: 300 BOTTLE in 1 BOX / 10 mL in 1 BOTTLE

NDC Code 52985-904-02

Package Description: 150 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE

NDC Code 52985-904-03

Package Description: 120 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE

NDC Code 52985-904-04

Package Description: 100 BOTTLE in 1 BOX / 100 mL in 1 BOTTLE

NDC Code 52985-904-05

Package Description: 30 BOTTLE in 1 BOX / 236 mL in 1 BOTTLE

NDC Code 52985-904-06

Package Description: 20 BOTTLE in 1 BOX / 350 mL in 1 BOTTLE

NDC Code 52985-904-07

Package Description: 24 BOTTLE in 1 BOX / 500 mL in 1 BOTTLE

NDC Code 52985-904-08

Package Description: 12 BOTTLE in 1 BOX / 1000 mL in 1 BOTTLE

NDC Code 52985-904-09

Package Description: 4 BOTTLE in 1 BOX / 3785 mL in 1 BOTTLE

NDC Code 52985-904-10

Package Description: 4 BOTTLE in 1 BOX / 5000 mL in 1 BOTTLE

NDC Code 52985-904-11

Package Description: 500 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE

NDC Code 52985-904-12

Package Description: 500 BOTTLE in 1 BOX / 20 mL in 1 BOTTLE

NDC Code 52985-904-13

Package Description: 400 BOTTLE in 1 BOX / 25 mL in 1 BOTTLE

NDC Code 52985-904-14

Package Description: 300 BOTTLE in 1 BOX / 38 mL in 1 BOTTLE

NDC Code 52985-904-15

Package Description: 150 BOTTLE in 1 BOX / 55 mL in 1 BOTTLE

Product Details

What is NDC 52985-904?

The NDC code 52985-904 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Anhui Oasis Disinfection Products Co., Ltd. The product's dosage form is . The product is distributed in 15 packages with assigned NDC codes 52985-904-01 300 bottle in 1 box / 10 ml in 1 bottle, 52985-904-02 150 bottle in 1 box / 30 ml in 1 bottle, 52985-904-03 120 bottle in 1 box / 60 ml in 1 bottle, 52985-904-04 100 bottle in 1 box / 100 ml in 1 bottle, 52985-904-05 30 bottle in 1 box / 236 ml in 1 bottle, 52985-904-06 20 bottle in 1 box / 350 ml in 1 bottle, 52985-904-07 24 bottle in 1 box / 500 ml in 1 bottle, 52985-904-08 12 bottle in 1 box / 1000 ml in 1 bottle, 52985-904-09 4 bottle in 1 box / 3785 ml in 1 bottle, 52985-904-10 4 bottle in 1 box / 5000 ml in 1 bottle, 52985-904-11 500 bottle in 1 box / 15 ml in 1 bottle, 52985-904-12 500 bottle in 1 box / 20 ml in 1 bottle, 52985-904-13 400 bottle in 1 box / 25 ml in 1 bottle, 52985-904-14 300 bottle in 1 box / 38 ml in 1 bottle, 52985-904-15 150 bottle in 1 box / 55 ml in 1 bottle. 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 Hand Sanitizer?

■Apply small amount onto your palm, not on open wound■Rub all parts of hands until dry without rinse Children under 6 years of age should be supervised during use Other information Sore below 86°F (30°C) 1 May discolor certain fabrics or surfaces ■Use within 12 months after open

Which are Hand Sanitizer UNII Codes?

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

Which are Hand Sanitizer 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:

What is the NDC to RxNorm Crosswalk for Hand Sanitizer?

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".