Class II · Moderate risk
Betadine Solution Swabstick Povidone-Iodine Solution USP
Subpotent Drug
National Drug Code
Is NDC 67618-0153-01 recalled?
Betadine Solution Swabsticks
Yes — this exact package was recalled
2 FDA recalls name the code 67618-0153-01 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
- Povidone-Iodine
- Strength
- POVIDONE-IODINE 10 mg/mL
- Form
- Solution · Topical
- Labeler
- Atlantis Consumer Healthcare, Inc.
- Type
- Human OTC Drug
- Product code
- 67618-0153
Recalls naming this package
Class II · Moderate risk
Betadine Solution Swabstick Povidone-Iodine Solution USP
Subpotent Drug: The laminate used to make the pouches was reversed such that the aluminum layer was in contact with the product causing an exothermic reaction between the free iodine and the aluminum.
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
- 67618-0100 See recall 1
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