NDC 57955-6044 Asthma Symptom Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-6044 - Asthma Symptom Relief
Product Packages
NDC Code 57955-6044-2
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 59 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 57955-6044?
What are the uses for Asthma Symptom Relief?
Which are Asthma Symptom Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H)
- ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H) (Active Moiety)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
- GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
- GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4) (Active Moiety)
Which are Asthma Symptom Relief 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)
* 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".