NDC 57844-208 Galzin
Zinc Acetate Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57844 - Teva Pharmaceuticals Usa, Inc.
- 57844-208 - Galzin
Product Characteristics
ORANGE (C48331)
93;208;93;208
Product Packages
NDC Code 57844-208-52
Package Description: 250 CAPSULE in 1 BOTTLE
Product Details
What is NDC 57844-208?
What are the uses for Galzin?
What are Galzin Active Ingredients?
- ZINC ACETATE 50 mg/1 - A salt produced by the reaction of zinc oxide with acetic acid and used as an astringent, styptic, and emetic.
Which are Galzin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Galzin 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- SHELLAC (UNII: 46N107B71O)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
What is the NDC to RxNorm Crosswalk for Galzin?
- RxCUI: 199994 - zinc acetate 25 MG Oral Capsule
- RxCUI: 199995 - zinc acetate 50 MG Oral Capsule
- RxCUI: 213049 - GALZIN 25 MG Oral Capsule
- RxCUI: 213049 - zinc acetate 25 MG Oral Capsule [Galzin]
- RxCUI: 213049 - Galzin 25 MG Oral Capsule
Which are the Pharmacologic Classes for Galzin?
* Please review the disclaimer below.
Patient Education
Zinc
What is it? Zinc is an essential trace element commonly found in red meat, poultry, and fish. It is necessary in small amounts for human health, growth, and sense of taste.
Zinc is found throughout the body. The body doesn't store excess zinc, so it must be obtained from the diet. It's needed for immune function, wound healing, blood clotting, thyroid function, and much more. It also plays a key role in maintaining vision and might have effects against viruses.
People commonly use zinc for zinc deficiency, diarrhea, and Wilson disease. Zinc is also used for acne, diabetes, anorexia, burns, and many other purposes. There is some scientific evidence to support its use for some of these conditions. But for most, there is no good scientific evidence to support its use. There is also no good evidence to support using zinc for COVID-19.
[Learn More]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".