NDC 69243-1111 Idlife Sanitize Moisturizing Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69243 - Willspeed Technologies Llc
- 69243-1111 - Idlife Sanitize Moisturizing Hand Sanitizer
Product Packages
NDC Code 69243-1111-1
Package Description: 30 mL in 1 BOTTLE, PUMP
NDC Code 69243-1111-2
Package Description: 44 mL in 1 BOTTLE, PUMP
NDC Code 69243-1111-3
Package Description: 59 mL in 1 BOTTLE, PUMP
NDC Code 69243-1111-4
Package Description: 118 mL in 1 BOTTLE, PUMP
NDC Code 69243-1111-5
Package Description: 237 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69243-1111?
What are the uses for Idlife Sanitize Moisturizing Hand Sanitizer?
Which are Idlife Sanitize Moisturizing 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 Idlife Sanitize Moisturizing 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AVENA SATIVA LEAF (UNII: 206PI19V7R)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- SOY PROTEIN (UNII: R44IWB3RN5)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- JOJOBA OIL (UNII: 724GKU717M)
- SORBIC ACID (UNII: X045WJ989B)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Idlife Sanitize Moisturizing Hand Sanitizer?
- RxCUI: 1046442 - benzalkonium chloride 0.13 % Topical Lotion
- RxCUI: 1046442 - benzalkonium chloride 1.3 MG/ML Topical Lotion
* 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".