Mucus Relief Sinus
- Product NDC
- 63187-587
- 11-digit product format
- 631870587
- Labeler code
- 63187
- Product ID
- 63187-587_c7dd543a-68e4-48ef-8c8c-2ae1b6361f8d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Phenylephrine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2006-04-15
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 400 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 product | product | 63187-587 | D | Discontinued by firm | 2026-10-20 | ||
| excluded package | package | 63187-587 | 63187-587-30 | D | Discontinued by firm | 2026-10-20 | |
| excluded package | package | 63187-587 | 63187-587-60 | D | Discontinued by firm | 2026-10-20 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 63187-587-30 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 63187-587-60 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 63187-587-30 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 63187-587-60 | f5e01cc5f278… | a2eaf40c39c3… |
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 |
|---|---|---|---|---|---|---|---|
| 63187-587-30 | 63187058730 | 1 BOTTLE, PLASTIC in 1 CARTON (63187-587-30) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2015-12-01 | 0000-00-00 | No | No | Current |
| 63187-587-60 | 63187058760 | 1 BOTTLE, PLASTIC in 1 CARTON (63187-587-60) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2015-12-01 | 0000-00-00 | No | No | Current |