NDC 68071-4595 Motion-time Chewable
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4595 - Motion-time
Product Characteristics
Product Packages
NDC Code 68071-4595-2
Package Description: 20 TABLET, CHEWABLE in 1 BOTTLE
NDC Code 68071-4595-3
Package Description: 30 TABLET, CHEWABLE in 1 BOTTLE
NDC Code 68071-4595-4
Package Description: 40 TABLET, CHEWABLE in 1 BOTTLE
NDC Code 68071-4595-6
Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE
Product Details
What is NDC 68071-4595?
What are the uses for Motion-time Chewable?
Which are Motion-time Chewable UNII Codes?
The UNII codes for the active ingredients in this product are:
- MECLIZINE HYDROCHLORIDE (UNII: HDP7W44CIO)
- MECLIZINE (UNII: 3L5TQ84570) (Active Moiety)
Which are Motion-time Chewable 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CROSPOVIDONE (UNII: 68401960MK)
- DEXTROSE (UNII: IY9XDZ35W2)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- RASPBERRY (UNII: 4N14V5R27W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- VANILLA (UNII: Q74T35078H)
What is the NDC to RxNorm Crosswalk for Motion-time Chewable?
- RxCUI: 995632 - meclizine HCl 25 MG Chewable Tablet
- RxCUI: 995632 - meclizine hydrochloride 25 MG Chewable Tablet
* Please review the disclaimer below.
Patient Education
Meclizine
Meclizine is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is most effective if taken before symptoms appear.
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* 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".