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NDC 00363-7007-15 No Drip Anefrin Nasal 0.05 g/100mL Details

No Drip Anefrin Nasal 0.05 g/100mL

No Drip Anefrin Nasal is a NASAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by WALGREENS. The primary component is OXYMETAZOLINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Oxymetazoline nasal spray is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Oxymetazoline nasal spray should not be used to treat children younger than 6 years of age unless it is recommended by a doctor. Children 6 to 12 years of age should use oxymetazoline nasal spray carefully and under adult supervision. Oxymetazoline is in a class of medications called nasal decongestants. It works by narrowing the blood vessels in the nasal passages.

Related Packages: 00363-7007-15
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Oxymetazoline Nasal Spray

Product Information

NDC	00363-7007
Product ID	0363-7007_bbf0dc69-c2d0-385e-e053-2995a90af9ee
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	No Drip Anefrin Nasal
Proprietary Name Suffix	n/a
Non-Proprietary Name	OXYMETAZOLINE HYDROCHLORIDE
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	NASAL
Active Ingredient Strength	0.05
Active Ingredient Units	g/100mL
Substance Name	OXYMETAZOLINE HYDROCHLORIDE
Labeler Name	WALGREENS
Pharmaceutical Class	Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part341
Listing Certified Through	2022-12-31

Package

Package Images

NDC 00363-7007-15 (00363700715)

Pricing Information	N/A
NDC Package Code	0363-7007-15
Billing NDC	00363700715
Package	15 mL in 1 BOTTLE (0363-7007-15)
Marketing Start Date	2021-02-26
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL b6234e99-115f-6018-e053-2a95a90a6989 Details

Drug Facts

ACTIVE INGREDIENT

Oxymetazoline hydrochloride 0.05%

Purpose

Nasal decongestant

Uses

temporaily relieves nasal congestion due to:
common cold
hay fever
upper respiratory allergires
temporarily relieves sinus congestion and pressure
shrinks swollen nasal membranes so you can breath more freely

Warnings

Ask a doctor before use if you have

heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostrate gland

When using this product

do not use more than directed
do not use for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen.
temporary discomfort such as buring, stinging, sneezing or an increase in nasal discharge may occur
use of this container by more than one person may spread infection

Stop use and ask a doctor if symptoms persist

If pregnant or breast-feeding, ask a health professional before use.

SPL UNCLASSIFIED SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period.
childer under 6 years of age: ask a doctor.

To Use: Shake well before use. Hold white tabs, press grooved area of cap firmly and turn counter clockwise. Before using for the first time, prime metered pump by depressing firmly several times. To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozel clean after use.

Secure cap after use.

Other information

store between 20º to 25ºC (68º to 77ºF)
retain carton for future reference on full labeling

Inactive ingredients

benzalkonium chloride solution, carboxymethylcellulose sodium solution, edetate disodium, glycerin, microcrystalline cellulose, polyethylene glycol 300, povidone, propylene glycol, purified water, sodium phosphate dibasic, sodium phosphate monobasic

Questions or comments?

1-800-925-4733

15 mL Bottle Carton

Anefrin Nasal Spray

NO DRIP

ORGINIAL

12 HOUR

MAXIMUM STRENGTH

Won't drip from nose or down throat
Helps Relieve congestion

0.5 FL OZ (15 mL)

INGREDIENTS AND APPEARANCE

NO DRIP ANEFRIN NASAL

oxymetazoline hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-7007
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	0.05 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
GLYCERIN (UNII: PDC6A3C0OX)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
POVIDONE K30 (UNII: U725QWY32X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-7007-15	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	02/26/2021

Labeler - WALGREENS (008965063)

Registrant - MEDICAL PRODUCTS LABORATORIES, INC. (002290302)

Name	Address	ID/FEI	Business Operations
Establishment
MEDICAL PRODUCTS LABORATORIES, INC.		002290302	manufacture(0363-7007)

Revised: 2/2021

Document Id: bbf0dc69-c2d0-385e-e053-2995a90af9ee

Set id: b6234e99-115f-6018-e053-2a95a90a6989

Version: 2

Effective Time: 20210226