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  4. NDC Product Code: 50260-200 Hand Sanitizer

NDC 50260-200 Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50260-200?
  5. Hand Sanitizer Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50260-200
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fercy Personal Care Products Co Limited
Labeler Code:
50260
Product Label ID:
bb74eac4-526d-4979-a0e6-6281b8c111a6
Start Marketing Date: [9]
02-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
GREEN (C48329)
RED (C48326)
PINK (C48328)
YELLOW (C48330)
Flavor(s):
APPLE (C73362)
BANANA (C73364)
BERRY (C73365)
GRAPE (C73391)
CHERRY (C73375)
MANGO (C73400)
LEMON (C73396)
BLUEBERRY (C73367)
PEACH (C73407)
STRAWBERRY (C73417)
ORANGE (C73406)
WATERMELON (C73423)

Product Packages

NDC Code 50260-200-01

Package Description: 5 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-02

Package Description: 8 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-03

Package Description: 10 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-04

Package Description: 20 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-05

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-06

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-07

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-08

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-09

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-10

Package Description: 240 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-11

Package Description: 360 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-12

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 50260-200-13

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 50260-200?

The NDC code 50260-200 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Fercy Personal Care Products Co Limited. The product's dosage form is . The product is distributed in 13 packages with assigned NDC codes 50260-200-01 5 ml in 1 bottle, plastic , 50260-200-02 8 ml in 1 bottle, plastic , 50260-200-03 10 ml in 1 bottle, plastic , 50260-200-04 20 ml in 1 bottle, plastic , 50260-200-05 30 ml in 1 bottle, plastic , 50260-200-06 50 ml in 1 bottle, plastic , 50260-200-07 60 ml in 1 bottle, plastic , 50260-200-08 100 ml in 1 bottle, plastic , 50260-200-09 120 ml in 1 bottle, plastic , 50260-200-10 240 ml in 1 bottle, plastic , 50260-200-11 360 ml in 1 bottle, plastic , 50260-200-12 500 ml in 1 bottle, plastic , 50260-200-13 1000 ml in 1 bottle, plastic . 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?

Wet hands thoroughly with product and rub hands together until dry. No need to wash or rinse your handsor use towels.Supervise children under 6 years of age.

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:

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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".