Class II · Moderate risk
McKesson Skin Protectant
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
National Drug Code
Is NDC 68599-6202-01 recalled?
Skin Protectant with Lanolin
Yes — this exact package was recalled
1 FDA recall names the code 68599-6202-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Lanolin
- Strength
- LANOLIN 50 g/100g
- Form
- Cream · Topical
- Labeler
- McKesson Medical-Surgical Inc.
- Type
- Human OTC Drug
- Product code
- 68599-6202
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
- 68599-6203 Skin Protectant with Lanolin 1
Free recall alerts
Know the day your medication is recalled
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