Chlorphen-12

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: Chlorphen-12
Generic name: CHLORPHENIRAMINE MALEATE
Manufacturer: KVK-Tech, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 84409269-fe9b-469e-9a66-27b1475231a3
SPL ID: 7d67f785-a25f-1819-e053-2991aa0a11d3
Version: 4
Effective date: 2018-12-19
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:51

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	040829	derived:openfda.application_number
application number		ANDA040829	openfda.application_number
brand name		Chlorphen-12	openfda.brand_name
generic name		CHLORPHENIRAMINE MALEATE	openfda.generic_name
manufacturer name		KVK-Tech, Inc.	openfda.manufacturer_name
ndc	package	10702-017-04	openfda.package_ndc
ndc	package	10702-017-54	openfda.package_ndc
ndc	package	10702-017-06	openfda.package_ndc
ndc	package	10702-017-24	openfda.package_ndc
ndc	package	10702-017-01	openfda.package_ndc
ndc	product	10702-017	openfda.product_ndc
ndc11	package	10702001701	derived:openfda.package_ndc
ndc11	package	10702001706	derived:openfda.package_ndc
ndc11	package	10702001704	derived:openfda.package_ndc
ndc11	package	10702001724	derived:openfda.package_ndc
ndc11	package	10702001754	derived:openfda.package_ndc
rxcui		1363288	openfda.rxcui
spl id		7d67f785-a25f-1819-e053-2991aa0a11d3	id
spl set id		84409269-fe9b-469e-9a66-27b1475231a3	set_id
unii		V1Q0O9OJ9Z	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 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 excitability may occur, especially in children drowsiness may occur avoid alcoholic beverages alchohol, sedatives and tranquilizers may increase drowsiness use caution when driving a motor vehicle or operating machinery Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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