Class II ยท Moderate risk
Alcohol Swabsticks
CGMP Deviations: products were stored outside the drug label specifications.
National Drug Code
Is NDC 67777-0300-01 recalled?
Alcohol · 10 BOX in 1 CASE (67777-300-01) / 50 POUCH in 1 BOX / 1.4 mL in 1 POUCH
Yes — this exact package was recalled
1 FDA recall names the code 67777-0300-01 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.
- Active ingredient
- Alcohol
- Strength
- ISOPROPYL ALCOHOL .7 mL/mL
- Form
- Swab · Topical
- Labeler
- Dynarex Corporation
- Type
- Human OTC Drug
- Product code
- 67777-0300
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
- 67777-0223 Zinc Oxide 1
- 67777-0234 Menthol and Zinc Oxide 1
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