HEB NASAL- phenylephrine hydrochloride spray

United States - English - NLM (National Library of Medicine)

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Active ingredient:
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)
Available from:
H E B
Administration route:
NASAL
Prescription type:
OTC DRUG
Therapeutic indications:
Nasal decongestant For the temporary relief of nasal congestion due to:
Authorization status:
OTC monograph final
Authorization number:
37808-728-30

HEB NASAL- phenylephrine hydrochloride spray

H E B

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

H.E.B. Nasal Spray Drug Facts

Active ingredient

Phenylephrine hydrochloride 1%

Purpos e

Nasal decongestant

Us es

For the temporary relief of nasal congestion due to:

Warnings

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

symptoms persist.

If pregnant or breast-feeding,

ask a health professional before use.

common cold

hay fever

upper respiratory allergies

heart disease

high blood pressure

thyroid disease

diabetes

trouble urinating due to an enlarged prostate gland

do not exceed recommended dosage

do not use for more than 3 days. use only as directed.

temporary discomfort such as burning, stinging, sneezing or an increase in nasal discharge may

occur

the use of this container by more than one person may spread infection

frequent or prolonged use may cause nasal congestion to recur or worsen

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222).

Directions

Other information

Inactive ingredients

benzalkonium chloride, benzyl alcohol, citric acid, purified water, sodium chloride, sodium citrate

Questions or comments?

1-866-467-2748

Principal Display Panel

Compare to 4-Way® Fast Acting Nasal Spray active ingredient*

NDC 37808-728-30

H.E.B

Nasal Spray

Phenylephrine Hydrochloride 1 %

Nasal Decongestant

Relief of:

1 FL OZ (30mL)

DO NOT USE IF PRINTED SEAL OVER CAP IS TORN OR MISSING

MADE WITH PRIDE & CARE FOR H-E-B

SAN ANTONIO, TX 78204

H-E-B®

100% GUARANTEE promise

adults and children 12 years of age & older: 2 or 3 sprays in each nostril not more often than

every 4 hours

children under 12 years of age: ask a doctor

Use instructions: with head in a normal, upright position, put atomizer tip into nostril. Squeeze

bottle with firm, quick pressure while inhaling. Wipe nozzle clean after each use.

store at room Temperature

container is filled to proper level for best spray action

Nasal Congestion

Sinus Congestion

Sinus Pressure

Swollen Nasal Membranes

If you aren’t completely pleases with this product, we’ll be happy to replace it or refund your money.

You have our word on it.

Keep this carton for future reference on full labeling.

*This product is not manufactured or distributed by Novartis Consumer Health, Inc.,

the owner of the registered trademark 4-Way

Fast Acting Nasal Spray.

HEB NASAL

phenylephrine hydrochloride spray

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:378 0 8 -728

Route of Administration

NASAL

H E B

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

PHENYLEPHRINE HYDRO CHLO RIDE (UNII: 0 4JA59 TNSJ) (PHENYLEPHRINE -

UNII:1WS29 7W6 MV)

PHENYLEPHRINE

HYDROCHLORIDE

in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7)

BENZYL ALCO HO L (UNII: LKG8 49 4WBH)

ANHYDRO US CITRIC ACID (UNII: XF417D3PSL)

WATER (UNII: 0 59 QF0 KO0 R)

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X)

SO DIUM CITRATE, UNSPECIFIED FO RM (UNII: 1Q73Q2JULR)

Product Characteristics

Color

YELLOW ((Clear to slightly yello w))

S core

S hap e

S iz e

Flavor

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:378 0 8 -728 -30

1 in 1 CARTON

0 3/14/20 19

1

30 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph final

pa rt341

0 3/14/20 19

Labeler -

H E B (007924756)

Revised: 9/2020

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