Class II · Moderate risk
Proctofoam HC
cGMP deficiencies
National Drug Code
Is NDC 0037-6822-10 recalled?
Proctofoam Hc · 1 CANISTER in 1 CARTON (0037-6822-10) / 10 g in 1 CANISTER
Yes — this exact package was recalled
2 FDA recalls name the code 0037-6822-10 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
- pramoxine hydrochloride hydrocortisone acetate
- Strength
- PRAMOXINE HYDROCHLORIDE 100 mg/10g; HYDROCORTISONE ACETATE…
- Form
- Aerosol, Foam · Topical
- Labeler
- Viatris Specialty LLC
- Type
- Human Prescription Drug
- Product code
- 0037-6822
Recalls naming this package
Class II · Moderate risk
Proctofoam HC
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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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