motion sickness relief

Generic: meclizine hydrochloride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name motion sickness relief
Generic Name meclizine hydrochloride
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-356
Product ID 11673-356_3df6ca6b-8de9-4c46-e063-6294a90ab4e9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2025-11-05

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673356
Hyphenated Format 11673-356

Supplemental Identifiers

RxCUI
995666
UNII
HDP7W44CIO

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 meclizine hydrochloride (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (11673-356-08) / 8 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3df6ca6b-8de9-4c46-e063-6294a90ab4e9", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["36ba2950-4a09-e5de-e063-6394a90a1771"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (11673-356-08)  / 8 TABLET in 1 BLISTER PACK", "package_ndc": "11673-356-08", "marketing_start_date": "20251105"}], "brand_name": "Motion Sickness Relief", "product_id": "11673-356_3df6ca6b-8de9-4c46-e063-6294a90ab4e9", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "11673-356", "generic_name": "Meclizine Hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness Relief", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}