Class II ยท Moderate risk
parodontax WHITENING
Presence of Foreign Substance: possibility of the presence of metal in the product.
National Drug Code
Is NDC 0135-0601-01 recalled?
parodontax · 1 TUBE in 1 CARTON (0135-0601-01) / 96.4 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 0135-0601-01 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
- stannous fluoride
- Strength
- STANNOUS FLUORIDE 1.1 mg/g
- Form
- Paste · Dental
- Labeler
- Haleon US Holdings LLC
- Type
- Human OTC Drug
- Product code
- 0135-0601
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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