motion sickness relief
Generic: dimenhydrinate
Labeler: l.n.k. international, inc.Drug Facts
Product Profile
Brand Name
motion sickness relief
Generic Name
dimenhydrinate
Labeler
l.n.k. international, inc.
Dosage Form
TABLET
Routes
Active Ingredients
dimenhydrinate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50844-199
Product ID
50844-199_5508a574-f890-4292-a91d-23f7a6652e48
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M009
Listing Expiration
2026-12-31
Marketing Start
1992-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50844199
Hyphenated Format
50844-199
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (50844-199-02) / 6 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5508a574-f890-4292-a91d-23f7a6652e48", "openfda": {"upc": ["0350844199027"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["95aae32f-6b3f-469d-86a5-c201a53f862a"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50844-199-02) / 6 TABLET in 1 BLISTER PACK", "package_ndc": "50844-199-02", "marketing_start_date": "19921201"}], "brand_name": "Motion Sickness Relief", "product_id": "50844-199_5508a574-f890-4292-a91d-23f7a6652e48", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50844-199", "generic_name": "Dimenhydrinate", "labeler_name": "L.N.K. International, 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": "19921201", "listing_expiration_date": "20261231"}