Giltuss EX Expectorant
- Product NDC
- 65852-008
- 11-digit product format
- 658520008
- Labeler code
- 65852
- Product ID
- 65852-008_3f67ac3d-1504-3418-e063-6394a90a938f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Dextrum Laboratories Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-06-22
- Substance
- GUAIFENESIN
- Active strength
- 400 mg/10mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Giltuss EX Expectorant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GUAIFENESIN | 400 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 495W7451VQ |
| Rxcui | 310625 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65852-008-04 | Giltuss EX Expectorant | 118 mL in 1 BOTTLE, PLASTIC | SOLUTION | 118 | | 1 |
| 65852-008-04 | Giltuss EX Expectorant | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 65852-008-04 | 65852000804 | 1 BOTTLE, PLASTIC in 1 CARTON (65852-008-04) / 118 mL in 1 BOTTLE, PLASTIC | 2020-06-22 | No | No | Historical |