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NDC 00067-8204-01 Theraflu Flu Relief Max Strength 1000; 30 mg/30mL; mg/30mL Details

Theraflu Flu Relief Max Strength 1000; 30 mg/30mL; mg/30mL

Theraflu Flu Relief Max Strength is a ORAL SYRUP in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE.

MedlinePlus Drug Summary

Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Related Packages: 00067-8204-01
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Acetaminophen

Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.

Related Packages: 00067-8204-01
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Dextromethorphan

Product Information

NDC	00067-8204
Product ID	0067-8204_0324195f-506d-4747-990e-ad44e2a117d9
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Theraflu Flu Relief Max Strength
Proprietary Name Suffix	Daytime
Non-Proprietary Name	Acetaminophen, Dextromethorphan HBr
Product Type	HUMAN OTC DRUG
Dosage Form	SYRUP
Route	ORAL
Active Ingredient Strength	1000; 30
Active Ingredient Units	mg/30mL; mg/30mL
Substance Name	ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE
Labeler Name	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Pharmaceutical Class	Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part341
Listing Certified Through	2024-12-31

Package

NDC 00067-8204-01 (00067820401)

Pricing Information	N/A
NDC Package Code	0067-8204-01
Billing NDC	00067820401
Package	245.5 mL in 1 BOTTLE (0067-8204-01)
Marketing Start Date	2022-06-27
NDC Exclude Flag	N