Meijer Multi-Symptom Relief
- Product NDC
- 55651-250
- Requested package NDC
- 55651-250-01
- 11-digit product format
- 556510250
- Labeler code
- 55651
- Product ID
- 55651-250_f1a2bfe5-ef9f-92b7-e053-2995a90a4aa3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- polyethylene glycol, tetrahydrozoline hydrochloride, zinc sulfate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- K.C. Pharmaceuticals, Inc.
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2023-01-09
- Marketing end
- 0000-00-00
- Substance
- POLYETHYLENE GLYCOL 400; TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
- Active strength
- 1 g/100mL; g/100mL; g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 55651-250-01 | 55651025001 | 1 BOTTLE, DROPPER in 1 CARTON (55651-250-01) > 15 mL in 1 BOTTLE, DROPPER | 2023-01-09 | 0000-00-00 | No | No | Current |