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NDC 00363-1110-22 Allergy Relief D 4; 60 mg/1; mg/1 Details

Allergy Relief D 4; 60 mg/1; mg/1

Allergy Relief D is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Chlorpheniramine relieves red, itchy, watery eyes; sneezing; itchy nose or throat; and runny nose caused by allergies, hay fever, and the common cold. Chlorpheniramine helps control the symptoms of cold or allergies but will not treat the cause of the symptoms or speed recovery. Chlorpheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.

Related Packages: 00363-1110-22
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Chlorpheniramine

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

Related Packages: 00363-1110-22
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Pseudoephedrine

Product Information

NDC	00363-1110
Product ID	0363-1110_3835c8d5-f1c0-4d06-8ec9-794f124d1e48
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	Allergy Relief D
Proprietary Name Suffix	n/a
Non-Proprietary Name	Chlorpheniramine maleate, Pseudoephedrine HCl
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	4; 60
Active Ingredient Units	mg/1; mg/1
Substance Name	CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Labeler Name	Walgreen Company
Pharmaceutical Class	Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M012
Listing Certified Through	2024-12-31

Package

NDC 00363-1110-22 (00363111022)

Pricing Information	N/A
NDC Package Code	0363-1110-22
Billing NDC	00363111022
Package	2 BLISTER PACK in 1 CARTON (0363-1110-22) / 24 TABLET in 1 BLISTER PACK
Marketing Start Date	2021-08-24
NDC Exclude Flag	N