Class II · Moderate risk
Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant
cGMP deviations
National Drug Code
Is NDC 69396-0086-02 recalled?
Zinc Oxide 20% · 1 TUBE in 1 BOX (69396-086-02) / 60 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 69396-0086-02 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
- Strength
- ZINC OXIDE .2 g/g
- Form
- Ointment · Topical
- Labeler
- Trifecta Pharmaceuticals USA
- Type
- Human OTC Drug
- Product code
- 69396-0086
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
- 69396-0087 Clotrimazole 2
Free recall alerts
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