NDC 49288-9933 Sterile Diluent For Allergenic Extract
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-9933 - Sterile Diluent For Allergenic Extract
Product Packages
NDC Code 49288-9933-1
Package Description: 2 mL in 1 VIAL
NDC Code 49288-9933-2
Package Description: 4 mL in 1 VIAL
NDC Code 49288-9933-3
Package Description: 4.5 mL in 1 VIAL
NDC Code 49288-9933-4
Package Description: 8 mL in 1 VIAL
NDC Code 49288-9933-5
Package Description: 9 mL in 1 VIAL
NDC Code 49288-9933-6
Package Description: 24 mL in 1 VIAL
NDC Code 49288-9933-7
Package Description: 30 mL in 1 VIAL
NDC Code 49288-9933-8
Package Description: 100 mL in 1 VIAL
NDC Code 49288-9933-9
Package Description: 40 mL in 1 VIAL
Product Details
What is NDC 49288-9933?
What are the uses for Sterile Diluent For Allergenic Extract?
Which are Sterile Diluent For Allergenic Extract UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
Which are Sterile Diluent For Allergenic Extract 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)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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[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".