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NDC 00135-7031-01 Panadol 325; 5 mg/1; mg/1 Details

Panadol 325; 5 mg/1; mg/1

Panadol is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and 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: 00135-7031-01
Last Updated: 02/05/2023
MedLinePlus Full Drug Details: Acetaminophen

Phenylephrine is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.

Related Packages: 00135-7031-01
Last Updated: 02/05/2023
MedLinePlus Full Drug Details: Phenylephrine

Product Information

NDC	00135-7031
Product ID	0135-7031_31ba233e-eeaf-4124-822c-87faffb98ca3
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	Panadol
Proprietary Name Suffix	Cold and Flu NonDrowsy
Non-Proprietary Name	acetaminophen and phenyleprine HCl
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	325; 5
Active Ingredient Units	mg/1; mg/1
Substance Name	ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Labeler Name	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Pharmaceutical Class	Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part341
Listing Certified Through	2024-12-31

Package

NDC 00135-7031-01 (00135703101)

Pricing Information	N/A
NDC Package Code	0135-7031-01
Billing NDC	00135703101
Package	50 PACKET in 1 CARTON (0135-7031-01) / 2 TABLET, FILM COATED in 1 PACKET
Marketing Start Date	2022-12-20
NDC Exclude Flag	N