NDC 29500-9711 Touch Free Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 29500 - Personal Care Products
- 29500-9711 - Touch Free Hand
Product Packages
NDC Code 29500-9711-1
Package Description: 251 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 29500-9711?
What are the uses for Touch Free Hand?
Which are Touch Free Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Touch Free Hand 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- CITRIC ACID (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Touch Free Hand?
- RxCUI: 1039026 - benzethonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1039026 - benzethonium chloride 1.3 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
[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".