Class II · Moderate risk
Dynashield
cGMP deviations
National Drug Code
Is NDC 67777-0407-03 recalled?
Dynashield
Yes — this exact package was recalled
1 FDA recall names the code 67777-0407-03 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.
2 of these recalls are still ongoing.
- Active ingredient
- zinc oxide
- Strength
- ZINC OXIDE 1.8 g/100g
- Form
- Cream · Topical
- Labeler
- Dynarex Corporation
- Type
- Human OTC Drug
- Product code
- 67777-0407
Recalls naming this package
Class II · Moderate risk
Dynashield Skin Protectant
cGMP deviations
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
- 67777-0120 See recall 1
- 67777-0121 Alcohol Prep 1
- 67777-0223 Zinc Oxide 1
- 67777-0234 Menthol and Zinc Oxide 1
- 67777-0244 BZK Pads 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.