Class II · Moderate risk
Clindamycin Phosphate and Benzoyl Peroxide Gel
Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
National Drug Code
Is NDC 45802-0736-84 recalled?
clindamycin phosphate and benzoyl peroxide · 1 TUBE in 1 CARTON (45802-736-84) / 45 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 45802-0736-84 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
- Clindamycin, Benzoyl Peroxide
- Strength
- CLINDAMYCIN PHOSPHATE 10 mg/g; BENZOYL PEROXIDE 50 mg/g
- Form
- Gel · Topical
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Type
- Human Prescription Drug
- Product code
- 45802-0736
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
- 45802-0425 See recall 2
- 45802-0571 See recall 2
- 45802-0868 Polyethylene Glycol 3350 2
- 45802-0014 Hydrocortisone 1
- 45802-0054 Triamcinolone Acetonide 1
- 45802-0059 Nystatin 1
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