NDC 75306-004 Prosera Soothing 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:
75306-004
Proprietary Name:
Prosera Soothing Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
D-time Limited Liability Company
Labeler Code:
75306
Start Marketing Date: [9]
05-21-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 75306-004-01

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-02

Package Description: 50 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-03

Package Description: 60 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-04

Package Description: 100 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-05

Package Description: 120 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-06

Package Description: 150 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-07

Package Description: 160 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-08

Package Description: 200 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-09

Package Description: 250 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-10

Package Description: 500 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-11

Package Description: 1000 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-12

Package Description: 3785 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-13

Package Description: 18927 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-14

Package Description: 5000 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-15

Package Description: 10000 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-16

Package Description: 15000 mL in 1 BOTTLE, SPRAY

NDC Code 75306-004-17

Package Description: 20000 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 75306-004?

The NDC code 75306-004 is assigned by the FDA to the product Prosera Soothing Hand Sanitizer which is product labeled by D-time Limited Liability Company. The product's dosage form is . The product is distributed in 17 packages with assigned NDC codes 75306-004-01 30 ml in 1 bottle, spray , 75306-004-02 50 ml in 1 bottle, spray , 75306-004-03 60 ml in 1 bottle, spray , 75306-004-04 100 ml in 1 bottle, spray , 75306-004-05 120 ml in 1 bottle, spray , 75306-004-06 150 ml in 1 bottle, spray , 75306-004-07 160 ml in 1 bottle, spray , 75306-004-08 200 ml in 1 bottle, spray , 75306-004-09 250 ml in 1 bottle, spray , 75306-004-10 500 ml in 1 bottle, spray , 75306-004-11 1000 ml in 1 bottle, spray , 75306-004-12 3785 ml in 1 bottle, spray , 75306-004-13 18927 ml in 1 bottle, spray , 75306-004-14 5000 ml in 1 bottle, spray , 75306-004-15 10000 ml in 1 bottle, spray , 75306-004-16 15000 ml in 1 bottle, spray , 75306-004-17 20000 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 Prosera Soothing Hand Sanitizer?

Adults and children over 2 years: ∙ For occasional and personal domestic use ∙ Supervise children when they use this product ∙ Spray onto hands and rub thoroughly for at least 30 seconds. Allow to dry.

Which are Prosera Soothing Hand Sanitizer UNII Codes?

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

Which are Prosera Soothing 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 Prosera Soothing 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:

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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".