Class II ยท Moderate risk
No Drip Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 41163-0703-10 recalled?
equaline nasal · 1 BOTTLE, PUMP in 1 CARTON (41163-703-10) / 30 mL in 1 BOTTLE, PUMP
Yes — this exact package was recalled
1 FDA recall names the code 41163-0703-10 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Oxymetazoline HCl
- Strength
- OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL
- Form
- Spray, Metered · Nasal
- Labeler
- United Natural Foods, Inc. dba UNFI
- Type
- Human OTC Drug
- Product code
- 41163-0703
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 41163-0769 citroma 2
- 41163-0129 Equaline Extra Strength Assorted Berry Antacid 1
- 41163-0171 EQU Ultra Strength Antacid Assorted Fruit 171AF 1
- 41163-0343 Equaline Nasal 1
- 41163-0404 See recall 1
- 41163-0458 Equaline all day allergy 1
Free recall alerts
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