NDC 77849-002 Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77849 - Yangzhou Eco-amenities Co., Ltd
- 77849-002 - Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol
Product Packages
NDC Code 77849-002-02
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 77849-002?
What are the uses for Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol?
Which are Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol 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)
- DICHLOROBENZYL ALCOHOL (UNII: 1NKX3648J9)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOCOPHEROL (UNII: R0ZB2556P8)
What is the NDC to RxNorm Crosswalk for Terra Pure Spa Collection Fresh Aloe Hand Sanitizer 75 Alcohol?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
* 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".