NDC 77731-045 Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77731 - Argento Sc By Sicura Inc.
- 77731-045 - Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack
Product Packages
NDC Code 77731-045-01
Package Description: 1 KIT in 1 BOX * 2 BOTTLE in 1 PACKAGE (77731-043-02) / 354 mL in 1 BOTTLE * 2 BOTTLE in 1 PACKAGE (77731-044-02) / 354 mL in 1 BOTTLE
Product Details
What is NDC 77731-045?
What are the uses for Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack?
Which are Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack 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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Purelogic Hand Sanitizer Soothing Gel And Soothing Aloe 6 Pack?
- RxCUI: 1094724 - ethanol 63 % Topical Gel
- RxCUI: 1094724 - ethanol 0.63 ML/ML Topical Gel
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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".