NDC 54557-0002 Bruises Gone Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54557 - Medcare Group Llc
- 54557-0002 - Bruises Gone Gel
Product Packages
NDC Code 54557-0002-1
Package Description: 60 mL in 1 TUBE
Product Details
What is NDC 54557-0002?
What are the uses for Bruises Gone Gel?
Which are Bruises Gone Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
Which are Bruises Gone Gel 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:
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
- TROMETHAMINE (UNII: 023C2WHX2V)
* 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".