NDC 52904-460 Allergy Antihistamine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52904 - Select Corporation
- 52904-460 - Allergy Antihistamine
Product Characteristics
Product Packages
NDC Code 52904-460-02
Package Description: 2 TABLET in 1 PACKET
Product Details
What is NDC 52904-460?
What are the uses for Allergy Antihistamine?
Which are Allergy Antihistamine UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
Which are Allergy Antihistamine 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:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE (UNII: J2B2A4N98G)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
What is the NDC to RxNorm Crosswalk for Allergy Antihistamine?
- RxCUI: 1049630 - diphenhydrAMINE HCl 25 MG Oral Tablet
- RxCUI: 1049630 - diphenhydramine hydrochloride 25 MG Oral Tablet
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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".