Antigrip Cough and Cold

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
Antigrip Cough and Cold
Generic name
ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR
Manufacturer
Pharmadel LLC
Product type
HUMAN OTC DRUG
SPL set ID
3b53e5fc-f258-c2b9-e063-6394a90ab500
SPL ID
3b53e5fc-f257-c2b9-e063-6394a90ab500
Version
1
Effective date
2025-08-01
Source export date
2026-10-12
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:13:07
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if adult takes more than 4 doses in 24 hours , which is the maximum daily amount for this product child takes more than 5 doses in 24 hours taken with other drugs containing acetaminophen adult has 3 or more alcoholic drinks everyday while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away. Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking prescription monoamine oxidase inhibitors (MAOI) (certain drugs for depression, psychiatric, or emotional conditions or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask your doctor or pharmacist before taking this product. Ask a doctor before use if the user is a child with pain from arthritis has liver disease has glaucoma has a breathing problem such as emphysema or chronic bronchitis has difficulty in urination due to enlargement of the prostate gland has a persistent or chronic cough such as occurs with smoking, asthma, or emphysema has a cough that is accompanied by excessive phlegm (mucus) is taking sedatives or tranquilizers Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin When using this product may cause marked drowsiness may cause excitability, especially in children may cause drowsiness; alcohol, sedatives, and tranquilizers may increase the drowsiness effect avoid alcoholic beverages while taking this product use caution when driving a motor vehicle or operating machinery Stop use and ask a doctor If pain or cough gets worse or lasts more than 5 days (children) or 7 days (adults) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur a cough comes back or occurs with a rash headache that lasts. These could be signs of a serious condition. If pregnant or breast-feeding , ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. In case of an accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Reported adverse events (FAERS/openFDA)#

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