Class III ยท Low risk
Nicotine Transdermal System Patch
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
National Drug Code
Is NDC 0536-5895-88 recalled?
Nicotine · 14 POUCH in 1 CARTON (0536-5895-88) / 1 h in 1 POUCH
Yes — this exact package was recalled
1 FDA recall names the code 0536-5895-88 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.
1 of these recalls is still ongoing.
- Active ingredient
- Nicotine
- Strength
- NICOTINE 14 mg/24h
- Form
- Patch · Transdermal
- Labeler
- Rugby Laboratories
- Type
- Human OTC Drug
- Product code
- 0536-5895
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
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