Theraflu Expressmax Daytime Severe Cold and Cough and Theraflu Expressmax Nighttime Severe Cold and Cough
- Product NDC
- 0067-8138
- 11-digit product format
- 000678138
- Labeler code
- 0067
- Product ID
- 0067-8138_bf2f5e57-ca6d-4cd9-b851-b12ae84ef476
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan HBr, phenylephrine HCl, diphenhydramine HCl
- Dosage form
- KIT
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-07-05
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0067-8138-40 | 00067813840 | 1 KIT in 1 CARTON (0067-8138-40) * 2 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2016-07-05 | 0000-00-00 | No | No | Current |