Class II · Moderate risk
H-E-B
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
National Drug Code
Is NDC 37808-0809-09 recalled?
inControl alcohol · 1 APPLICATOR in 1 PACKET (37808-809-09) / 5 mL in 1 APPLICATOR
Yes — this exact package was recalled
1 FDA recall names the code 37808-0809-09 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
- Isopropyl Alcohol
- Strength
- ISOPROPYL ALCOHOL 70 mL/100mL
- Form
- Swab · Topical
- Labeler
- H-E-B
- Type
- Human OTC Drug
- Product code
- 37808-0809
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
- 37808-0196 See recall 2
- 37808-0507 See recall 2
- 37808-0876 See recall 2
- 37808-0136 HEB Extra Stregth Antacid 1
- 37808-0161 Pain and Fever 1
- 37808-0288 See recall 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.