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NDC 49035-0131-62 Equate Suphedrine PE 10 mg/1 Details

Equate Suphedrine PE 10 mg/1

Equate Suphedrine PE is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores Inc. The primary component is PHENYLEPHRINE HYDROCHLORIDE.

MedlinePlus Drug Summary

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: 49035-0131-62
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Phenylephrine

Product Information

NDC	49035-0131
Product ID	49035-131_04ff8857-8512-4130-a213-b488617ad55e
Associated GPIs	49200020100303
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	Equate Suphedrine PE
Proprietary Name Suffix	n/a
Non-Proprietary Name	Phenylephrine Hydrochloride
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	10
Active Ingredient Units	mg/1
Substance Name	PHENYLEPHRINE HYDROCHLORIDE
Labeler Name	Wal-Mart Stores Inc
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

Package Images

NDC 49035-0131-62 (49035013162)

Pricing Information	N/A
NDC Package Code	49035-131-62
Billing NDC	49035013162
Package	24 BLISTER PACK in 1 CARTON (49035-131-62) / 1 TABLET in 1 BLISTER PACK
Marketing Start Date	2016-07-19
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 6bcf3e91-040b-4ed0-9cb9-2f7d67360667 Details

Active ingredient (in each tablet)

Phenylephrine HCl 10 mg

Purpose

Nasal decongestant

Uses

•: temporarily relieves sinus congestion and pressure
•: temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies

Warnings

Do not use

if you are now taking a prescription monoamine oxidase inhibitor (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 a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

•: heart disease
•: high blood pressure
•: thyroid disease
•: trouble urinating due to an enlarged prostate gland
•: diabetes

When using this product

do not exceed recommended dosage

Stop use and ask a doctor if

•: nervousness, dizziness, or sleeplessness occur
•: symptoms do not improve within 7 days or occur with a fever

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

adults and children 12 years and over	• take 1 tablet every 4 hours • do not take more than 6 tablets in 24 hours
children under 12 years	ask a doctor

Other information

•: store at 20-25ºC (68-77ºF)
•: do not use if blister unit is broken or torn

Inactive ingredients

anhydrous dibasic calcium phosphate, carnauba wax, FD&C red no. 40 aluminum lake, lecithin, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, talc, titanium dioxide

Questions or comments?

1-888-287-1915

Principal Display Panel

Compare to Sudafed PE® Congestion Active Ingredient

Congestion

Suphedrine PE

Phenylephrine HCl Tablets, 10 mg

Nasal Decongestant

Non-Drowsy

Relieves:

Sinus Pressure

Congestion

Maximum Strength

10 mg

24 TABLETS

Actual Size

INGREDIENTS AND APPEARANCE

EQUATE SUPHEDRINE PE

phenylephrine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-131
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	10 mg

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
CARNAUBA WAX (UNII: R12CBM0EIZ)

Product Characteristics
Color	RED	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	L7
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:49035-131-89	18 in 1 CARTON	03/21/2014	03/14/2018
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:49035-131-68	36 in 1 CARTON	03/21/2014	03/14/2018
2		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:49035-131-62	24 in 1 CARTON	07/19/2016
3		1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	03/21/2014

Labeler - Wal-Mart Stores Inc (051957769)

Revised: 11/2019

Document Id: 04ff8857-8512-4130-a213-b488617ad55e

Set id: 6bcf3e91-040b-4ed0-9cb9-2f7d67360667

Version: 5

Effective Time: 20191122