NDC 73401-850 Previcare Holy Water Plus Hyssop Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73401 - Previcare Pharmaceutical, Inc.
- 73401-850 - Previcare
Product Packages
NDC Code 73401-850-09
Package Description: 60 mL in 1 BOTTLE
NDC Code 73401-850-10
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 73401-850?
What are the uses for Previcare Holy Water Plus Hyssop Sanitizer?
Which are Previcare Holy Water Plus Hyssop Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Previcare Holy Water Plus Hyssop 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- HYSSOP OIL (UNII: 173D71924B)
What is the NDC to RxNorm Crosswalk for Previcare Holy Water Plus Hyssop Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".