NDC 0924-1007 Dimenhydrinate
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Product Details
What is NDC 0924-1007?
What are the uses for Dimenhydrinate?
Which are Dimenhydrinate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMENHYDRINATE (UNII: JB937PER5C)
- CHLORTHEOPHYLLINE (UNII: GE2UA340FM) (Active Moiety)
Which are Dimenhydrinate 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:
- CROSCARMELLOSE (UNII: 029TFK992N)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Dimenhydrinate?
- RxCUI: 198603 - dimenhyDRINATE 50 MG Oral Tablet
- RxCUI: 198603 - dimenhydrinate 50 MG Oral Tablet
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Patient Education
Dimenhydrinate
Dimenhydrinate is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. Dimenhydrinate is in a class of medications called antihistamines. It works by preventing problems with body balance.
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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".