Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0135-0651-02 recalled?

Parodontax Active Gum Health Mint · 500 mL in 1 BOTTLE (0135-0651-02)

Yes — this exact package was recalled

1 FDA recall names the code 0135-0651-02 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
cetylpyridinium chloride
Strength
CETYLPYRIDINIUM CHLORIDE 70 mg/mL
Form
Mouthwash · Oral
Labeler
Haleon US Holdings LLC
Type
Human OTC Drug
Product code
0135-0651

Recalls naming this package

Class III ยท Low risk

parodontax

Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.

Ongoing Labeling / mix-up Haleon US Holdings LLC NDC 0135-0651-02 D-0297-2026

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