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NDC 51672-2030-03 Oxymetazoline Hydrochloride 0.05 g/100mL Details
Oxymetazoline Hydrochloride 0.05 g/100mL
Oxymetazoline Hydrochloride is a NASAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. 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: 51672-2030-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Oxymetazoline Nasal Spray
Product Information
| NDC | 51672-2030 |
|---|---|
| Product ID | 51672-2030_b6e8883a-066f-44a5-ab4e-fe507bbf861d |
| Associated GPIs | 42102040102010 |
| 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 | Oxymetazoline Hydrochloride |
| Proprietary Name Suffix | 12-Hour |
| Non-Proprietary Name | Oxymetazoline Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | SPRAY |
| Route | NASAL |
| Active Ingredient Strength | 0.05 |
| Active Ingredient Units | g/100mL |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| 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 | 2024-12-31 |
Package
NDC 51672-2030-03 (51672203003)
| NDC Package Code | 51672-2030-3 |
|---|---|
| Billing NDC | 51672203003 |
| Package | 1 BOTTLE, SPRAY in 1 CARTON (51672-2030-3) / 30 mL in 1 BOTTLE, SPRAY |
| Marketing Start Date | 2006-02-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |