Maximum Strenth Nasal: Package Insert and Label Information

MAXIMUM STRENTH NASAL- oxymetazoline hydrochloride liquid

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.

Active ingredient Purpose

Oxymetazoline Hydrochloride — 0.05% Nazal Decongestant


For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies.


Do not use this product if person has heart disease, high blood pressure, thyroid disease, diabetes, or if adult has difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.

When using this product

Do not exceed recommended dosage

Do not use this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. If symptoms persist, consult a doctor.This product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge. The use of this container by more than one person may spread infection.

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


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. Children under 6 years of age: consult a doctor.

Inactive ingredients

Benzalkonium Chloride
Disodium EDTA
Polysorbate 80
Propylene Glycol
Sodium Chloride
Sodium Hydroxide

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oxymetazoline hydrochloride — 0.05% liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7003
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Oxymetazoline Hydrochloride (OXYMETAZOLINE) Oxymetazoline Hydrochloride 0.05 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Benzalkonium Chloride
Polysorbate 80
Propylene Glycol
Sodium Chloride
Sodium Hydroxide
# Item Code Package Description Multilevel Packaging
1 NDC:0363-7003-01 1 BOTTLE in 1 CARTON contains a BOTTLE
1 22 mL in 1 BOTTLE This package is contained within the CARTON (0363-7003-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 07/15/2016
Labeler — Walgreens (008965063)
Registrant — Product Quest Mfg. (927768135)
Name Address ID/FEI Operations
Product Quest Mfg. 927768135 manufacture (0363-7003), label (0363-7003)

Revised: 02/2018 Walgreens provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

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