NDC 81627-015 Bioshield 99
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81627 - Naturally Safe Solutions, Llc
- 81627-015 - Bioshield 99
Product Packages
NDC Code 81627-015-02
Package Description: 60 mL in 1 BOTTLE, SPRAY
NDC Code 81627-015-10
Package Description: 300 mL in 1 BOTTLE, SPRAY
NDC Code 81627-015-32
Package Description: 1000 mL in 1 BOTTLE, SPRAY
NDC Code 81627-015-50
Package Description: 3785 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 81627-015?
What are the uses for Bioshield 99?
Which are Bioshield 99 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- CINNAMON OIL (UNII: E5GY4I6YCZ) (Active Moiety)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
Which are Bioshield 99 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:
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
What is the NDC to RxNorm Crosswalk for Bioshield 99?
- RxCUI: 1241663 - ethanol 80 % Topical Spray
- RxCUI: 1241663 - ethanol 0.8 ML/ML Topical Spray
* 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".