NDC 70481-301 Hyr Hand Sanitizer With Aloe Vera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70481 - General Resources Llc
- 70481-301 - Hyr Hand Sanitizer With Aloe Vera
Product Packages
NDC Code 70481-301-05
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 70481-301-06
Package Description: 60 mL in 1 BOTTLE, PLASTIC
NDC Code 70481-301-24
Package Description: 250 mL in 1 BOTTLE, PLASTIC
NDC Code 70481-301-26
Package Description: 3800 mL in 1 BOTTLE, PLASTIC
NDC Code 70481-301-30
Package Description: 296 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 70481-301?
What are the uses for Hyr Hand Sanitizer With Aloe Vera?
Which are Hyr Hand Sanitizer With Aloe Vera UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Hyr Hand Sanitizer With Aloe Vera 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Hyr Hand Sanitizer With Aloe Vera?
- RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
- RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
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[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".