Class II · Moderate risk
Hydrocortisone Cream
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
National Drug Code
Is NDC 0363-0638-03 recalled?
Maximum Strength Hydrocortisone Cream · 1 TUBE in 1 CARTON (0363-0638-03) / 28 g in 1 TUBE (0363-0638-01)
Yes — this exact package was recalled
1 FDA recall names the code 0363-0638-03 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
- Hydrocortisone Cream
- Strength
- HYDROCORTISONE 1 g/100g
- Form
- Cream · Topical
- Labeler
- Walgreens
- Type
- Human OTC Drug
- Product code
- 0363-0638
Recalls naming this package
Class II · Moderate risk
Hydrocortisone Cream
CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.
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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