Mucus Relief
- Product NDC
- 55301-932
- 11-digit product format
- 553010932
- Labeler code
- 55301
- Product ID
- 55301-932_42c5e2d1-d6cc-43bc-acb5-18890a788b04
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ARMY AND AIR FORCE EXCHANGE SERVICE
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2005-12-22
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55301-932 | MUCUS RELIEF (GUAIFENESIN) TABLET, FILM COATED [ARMY AND AIR FORCE EXCHANGE SERVICE] | 5 | Legacy NDC | 20240829_3050af29-6522-4ec2-9230-deba56bffa2f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55301-932-91 | 55301093291 | 1 BOTTLE, PLASTIC in 1 CARTON (55301-932-91) > 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2005-12-22 | 0000-00-00 | No | No | Current |