NDC 77381-0001 Acqua Marina
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77381 - Think Italian Llc
- 77381-0001 - Acqua Marina
Product Packages
NDC Code 77381-0001-1
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 77381-0001-2
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 77381-0001-3
Package Description: 474 mL in 1 BOTTLE, PLASTIC
NDC Code 77381-0001-4
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 77381-0001-5
Package Description: 1774 mL in 1 BOTTLE, PLASTIC
NDC Code 77381-0001-6
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 77381-0001?
What are the uses for Acqua Marina?
Which are Acqua Marina UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Acqua Marina 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
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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".