Oxymetazoline Hydrochloride 51672-1405-02

Package NDC

51672-1405-02

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Cream
Route: Topical
Product Type: Human Prescription Drug
Marketing Start: July 15, 2026
Listing Expires: December 31, 2027
Application: ANDA213584

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Active Ingredients

Ingredient	Strength
Oxymetazoline Hydrochloride	10 mg/g

Drug Class

Imidazolines [CS]Increased Sympathetic Activity [PE]Vasoconstriction [PE]

Selected Package

51672-1405-02Selected

1 TUBE in 1 CARTON (51672-1405-2) / 30 g in 1 TUBE

Other packages for this product(1)

51672-1405-03

1 TUBE in 1 CARTON (51672-1405-3) / 60 g in 1 TUBE

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