Capron DMT

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: Capron DMT
Generic name: DEXTROMETHORPHAN HBR AND PYRILAMINE MALEATE
Manufacturer: Capital Pharma
Product type: HUMAN OTC DRUG
SPL set ID: 50222df4-5c31-1304-e054-00144ff88e88
SPL ID: 45a51318-64ac-dfca-e063-6394a90ab66e
Version: 6
Effective date: 2025-12-10
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:57:16

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Capron DMT	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR AND PYRILAMINE MALEATE	openfda.generic_name
manufacturer name		Capital Pharma	openfda.manufacturer_name
ndc	package	29978-128-10	openfda.package_ndc
ndc	product	29978-128	openfda.product_ndc
ndc11	package	29978012810	derived:openfda.package_ndc
rxcui		1923362	openfda.rxcui
spl id		45a51318-64ac-dfca-e063-6394a90ab66e	id
spl set id		50222df4-5c31-1304-e054-00144ff88e88	set_id
unii		R35D29L3ZA	openfda.unii
unii		9D2RTI9KYH	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

Do not exceed recommended dosage. May cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect. Avoid alcoholic beverages while taking this product. Do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor. Use caution when driving a motor vehicle or operating machinery.

Reported adverse events (FAERS/openFDA)#

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