Mucus Relief
- Product NDC
- 68016-545
- Requested package NDC
- 68016-545-50
- 11-digit product format
- 680160545
- Labeler code
- 68016
- Product ID
- 68016-545_d7e8bc98-a014-4d5a-bfdf-7274801bdb1c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chain Drug Consortium
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2023-01-09
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 68016-545 | 68016-545-50 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 68016-545-50 | 68016054550 | 1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50) > 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2023-01-09 | 0000-00-00 | No | No | Current |