Class II ยท Moderate risk
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cGMP deviations
National Drug Code
Is NDC 67777-0223-05 recalled?
Zinc Oxide
Yes — this exact package was recalled
1 FDA recall names the code 67777-0223-05 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
- Zinc Oxide Ointment
- Strength
- ZINC OXIDE 200 mg/g
- Form
- Ointment · Topical
- Labeler
- Dynarex Corporation
- Type
- Human OTC Drug
- Product code
- 67777-0223
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
- 67777-0245 BZK Pads 2
- 67777-0407 Dynashield 2
- 67777-0120 See recall 1
- 67777-0121 Alcohol Prep 1
- 67777-0234 Menthol and Zinc Oxide 1
- 67777-0244 BZK Pads 1
Free recall alerts
Know the day your medication is recalled
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