NDC 63083-2088 Gi Flu Symptom Drops 2088
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2088 - Gi Flu Symptom Drops
Product Packages
NDC Code 63083-2088-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2088?
What are the uses for Gi Flu Symptom Drops 2088?
Which are Gi Flu Symptom Drops 2088 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
- MARRUBIUM VULGARE WHOLE (UNII: 7A72MUN24Z)
- MARRUBIUM VULGARE WHOLE (UNII: 7A72MUN24Z) (Active Moiety)
- LEMON JUICE (UNII: AGN709ANTJ)
- LEMON JUICE (UNII: AGN709ANTJ) (Active Moiety)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) (Active Moiety)
- MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9)
- MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9) (Active Moiety)
- BASIL (UNII: 2U0KZP0FDW)
- BASIL (UNII: 2U0KZP0FDW) (Active Moiety)
- POPULUS BALSAMIFERA LEAF BUD (UNII: 9CQ6C00G3C)
- POPULUS BALSAMIFERA LEAF BUD (UNII: 9CQ6C00G3C) (Active Moiety)
- POGOSTEMON CABLIN TOP (UNII: 2I2A73IYL7)
- POGOSTEMON CABLIN TOP (UNII: 2I2A73IYL7) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I) (Active Moiety)
Which are Gi Flu Symptom Drops 2088 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".