NDC 57955-5121 Swollen Glands Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-5121 - Swollen Glands Relief
Product Packages
NDC Code 57955-5121-2
Package Description: 59 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 57955-5121?
What are the uses for Swollen Glands Relief?
Which are Swollen Glands Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASTACUS ASTACUS (UNII: V0551986XQ)
- ASTACUS ASTACUS (UNII: V0551986XQ) (Active Moiety)
- BARIUM IODIDE (UNII: WKC4T7680A)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- CALCIUM IODIDE (UNII: 8EKI9QEE2H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- CONIINE (UNII: C479P32L2D)
- CONIINE (UNII: C479P32L2D) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4)
- LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (Active Moiety)
- MERCURIC IODIDE (UNII: R03O05RB0P)
- MERCURIC IODIDE (UNII: R03O05RB0P) (Active Moiety)
- MERCURY (UNII: FXS1BY2PGL)
- MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
- SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
Which are Swollen Glands 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".