NDC 63083-2075 Travel Sickness Drops 2075
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2075 - Travel Sickness Drops
Product Packages
NDC Code 63083-2075-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2075?
What are the uses for Travel Sickness Drops 2075?
Which are Travel Sickness Drops 2075 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AETHUSA CYNAPIUM WHOLE (UNII: M6936L953C)
- AETHUSA CYNAPIUM WHOLE (UNII: M6936L953C) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- AMBERGRIS (UNII: XTC0D02P6C)
- AMBERGRIS (UNII: XTC0D02P6C) (Active Moiety)
- APOMORPHINE HYDROCHLORIDE (UNII: F39049Y068)
- APOMORPHINE (UNII: N21FAR7B4S) (Active Moiety)
- ANAMIRTA COCCULUS FRUIT (UNII: 3E8XBL6YYK)
- ANAMIRTA COCCULUS FRUIT (UNII: 3E8XBL6YYK) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J)
- LIQUID PETROLEUM (UNII: 6ZAE7X688J) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
Which are Travel Sickness Drops 2075 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".