motion sickness relief

Generic: dimenhydrinate

Labeler: chain drug marketing association, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name motion sickness relief
Generic Name dimenhydrinate
Labeler chain drug marketing association, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dimenhydrinate 50 mg/1

Manufacturer
Chain Drug Marketing Association, Inc.

Identifiers & Regulatory

Product NDC 83324-032
Product ID 83324-032_766ba325-4972-4feb-8ef9-39c824bd8f7e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2024-04-04

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324032
Hyphenated Format 83324-032

Supplemental Identifiers

RxCUI
198603
UPC
0635515997134
UNII
JB937PER5C

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name motion sickness relief (source: ndc)
Generic Name dimenhydrinate (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (83324-032-12) / 6 TABLET in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (83324-032-24) / 6 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

83324-032-12 2 BLISTER PACK in 1 CARTON (83324-032-12) / 6 TABLET in 1 BLISTER PACK 83324-032-24 4 BLISTER PACK in 1 CARTON (83324-032-24) / 6 TABLET in 1 BLISTER PACK

Ingredients (1)

dimenhydrinate (50 mg/1)

Linked Drug Pages (1)

Motion Sickness Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "766ba325-4972-4feb-8ef9-39c824bd8f7e", "openfda": {"upc": ["0635515997134"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["00a327c6-6b86-4702-8c04-55c405c1404c"], "manufacturer_name": ["Chain Drug Marketing Association, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (83324-032-12)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "83324-032-12", "marketing_start_date": "20240404"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (83324-032-24)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "83324-032-24", "marketing_start_date": "20240404"}], "brand_name": "Motion Sickness Relief", "product_id": "83324-032_766ba325-4972-4feb-8ef9-39c824bd8f7e", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83324-032", "generic_name": "Dimenhydrinate", "labeler_name": "Chain Drug Marketing Association, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness Relief", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}