NDC 58418-786 Skin Crave Non-alcohol Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58418 - Tropical Enterprises International, Inc.
- 58418-786 - Skin Crave Non-alcohol Hand Sanitizer
Product Packages
NDC Code 58418-786-00
Package Description: 10 mL in 1 PACKET
NDC Code 58418-786-01
Package Description: 30 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-02
Package Description: 60 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-04
Package Description: 120 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-05
Package Description: 15 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-08
Package Description: 240 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-10
Package Description: 10 mL in 1 BOTTLE, SPRAY
NDC Code 58418-786-12
Package Description: 360 mL in 1 BOTTLE, PUMP
NDC Code 58418-786-16
Package Description: 480 mL in 1 BOTTLE, PUMP
NDC Code 58418-786-17
Package Description: 50.275 mL in 1 BOTTLE, PUMP
NDC Code 58418-786-28
Package Description: 3840 mL in 1 BOTTLE, PUMP
NDC Code 58418-786-64
Package Description: 1920 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 58418-786?
What are the uses for Skin Crave Non-alcohol Hand Sanitizer?
Which are Skin Crave Non-alcohol Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Skin Crave Non-alcohol 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:
- 2-(2-(2-(2-PHENOXYETHOXY)ETHOXY)ETHOXY)ETHANOL (UNII: Y050HYR4XA)
* 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".