Class III ยท Low risk
Sankaijo BOTANICAL LAXATIVE
Subpotent Drug: Formulated amount of sennosides component is less than labelled claim.
National Drug Code
Is NDC 49873-0404-01 recalled?
Sankaijo · 1 BOTTLE in 1 CARTON (49873-404-01) / 150 TABLET in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 49873-0404-01 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
- docusate sodium, sennosides
- Strength
- DOCUSATE SODIUM 8.33 mg/1; SENNOSIDES 1.36 mg/1
- Form
- Tablet · Oral
- Labeler
- Sato Pharmaceutical Co., Ltd.
- Type
- Human OTC Drug
- Product code
- 49873-0404
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
- 49873-0020 See recall 1
- 49873-0044 See recall 1
- 49873-0402 Inon Ace 1
- 49873-0501 See recall 1
- 49873-0803 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.