Dramamine Less Drowsy

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Dramamine Less Drowsy
Generic name: MECLIZINE HYDROCHLORIDE
Manufacturer: Medtech Products Inc.
Product type: HUMAN OTC DRUG
SPL set ID: fa6a0969-7427-4b87-bc04-a2792665c218
SPL ID: 5aaed2b3-5738-2eaa-e063-6394a90a8f8b
Version: 7
Effective date: 2026-09-04
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:53

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M009	openfda.application_number
brand name		Dramamine Less Drowsy	openfda.brand_name
generic name		MECLIZINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Medtech Products Inc.	openfda.manufacturer_name
ndc	package	63029-903-04	openfda.package_ndc
ndc	package	63029-903-10	openfda.package_ndc
ndc	package	63029-903-01	openfda.package_ndc
ndc	package	63029-903-16	openfda.package_ndc
ndc	product	63029-903	openfda.product_ndc
ndc11	package	63029090310	derived:openfda.package_ndc
ndc11	package	63029090301	derived:openfda.package_ndc
ndc11	package	63029090304	derived:openfda.package_ndc
ndc11	package	63029090316	derived:openfda.package_ndc
rxcui		995726	openfda.rxcui
rxcui		995666	openfda.rxcui
spl id		5aaed2b3-5738-2eaa-e063-6394a90a8f8b	id
spl set id		fa6a0969-7427-4b87-bc04-a2792665c218	set_id
unii		HDP7W44CIO	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not give to children under 12 years of age unless directed by a doctor. Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery If pregnant or breast-feeding, ask a doctor before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.