Guaifenesin and Codeine Phosphate
- Product NDC
- 0121-1550
- 11-digit product format
- 001211550
- Labeler code
- 0121
- Product ID
- 0121-1550_2175415b-f07e-50a6-e063-6394a90acabe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin and Codeine Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- PAI Holdings, LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2006-10-01
- Substance
- GUAIFENESIN; CODEINE PHOSPHATE
- Active strength
- 200; 20 mg/10mL; mg/10mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Full Opioid Agonists [MoA], Increased Respiratory Secretions [PE], Opioid Agonist [EPC]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Guaifenesin and Codeine Phosphate
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 200 mg/10mL |
| CODEINE PHOSPHATE | 20 mg/10mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| GSL05Y1MN6 | Internal UNII lookup |
| 495W7451VQ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 995868 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 88d0994c-4270-4408-8837-bd97510b2118 | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0121-1550-00 | 2022-03-28 | C162847 | 48780-1 | d6a99b39-4ea2-a426-e053-dadaa90af4c2 | Guaifenesin and Codeine Phosphate |
| 0121-1550-00 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-4ea2-a426-e053-dadaa90af4c2 | Guaifenesin and Codeine Phosphate |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0121-1550-00 | Guaifenesin and Codeine Phosphate | 10 in 1 TRAY | SOLUTION | 10 | 11 | |
| 0121-1550-00 | Guaifenesin and Codeine Phosphate | 10 in 1 CASE | SOLUTION | 10 | 11 | |
| 0121-1550-10 | Guaifenesin and Codeine Phosphate | 10 mL in 1 CUP, UNIT-DOSE | SOLUTION | 10 | 11 | |
| 0121-1550-40 | Guaifenesin and Codeine Phosphate | 10 in 1 TRAY | SOLUTION | 10 | 11 | |
| 0121-1550-40 | Guaifenesin and Codeine Phosphate | 4 in 1 CASE | SOLUTION | 4 | 11 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0121-1550-00 | ML - Milliliter | 0121-1550 | b69d5b9d-f7c2-4d33-9f44-67c832179cf2 | 1 | 2017-08-11 |
| 0121-1550-10 | ML - Milliliter | 0121-1550 | dee23321-cef1-46cb-8d6c-347c5e81ccb6 | 1 | 2017-08-11 |
| 0121-1550-40 | ML - Milliliter | 0121-1550 | cdc60019-dabf-48fa-90f2-cd3a54928f5d | 1 | 2024-02-14 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Codeine Phosphate | ACTIVE INGREDIENT | GSL05Y1MN6 | GUAIFENESIN AND CODEINE PHOSPHATE SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.] | 1 | |
| Guaifenesin | ACTIVE INGREDIENT | 495W7451VQ | GUAIFENESIN AND CODEINE PHOSPHATE SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.] | 1 | |
| Codeine | ACTIVE MOIETY | Q830PW7520 | GUAIFENESIN AND CODEINE PHOSPHATE SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.] | 1 | |
| Guaifenesin | ACTIVE MOIETY | 495W7451VQ | GUAIFENESIN AND CODEINE PHOSPHATE SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.] | 1 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Severe Cold and Flu Night time | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | HyVee Inc | 4f963491-e1f0-494d-acb6-5f4d2b267d4a | 2026-04-22 | Warnings | M012 |
| Vicks Sinex SEVERE MOISTURIZING ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | f4b01827-7444-3bfc-e053-2a95a90aebed | 2026-04-22 | Warnings | M012 |
| Vicks Sinex SEVERE ORIGINAL ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH, | cfd43b8f-8064-6b88-e053-2a95a90a329e | 2026-04-22 | Warnings | M012 |
| Vicks Sinex Severe Original | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | cfd048c9-2f33-101d-e053-2995a90ad854 | 2026-04-22 | Warnings | M012 |
| Vicks Sinex SEVERE VapoCOOL ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | d0768332-7c24-7c30-e053-2a95a90a26d4 | 2026-04-22 | Warnings | M012 |
| Histanaz | PSEUDOEPHEDRINE HCL, PYRILAMINE MALEATE | Capital Pharmaceutical, LLC | 3e87d0f3-f16c-5972-e063-6294a90acc8a | 2026-04-22 | Warnings | M012 |
| Good Sense Severe Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | L. Perrigo Company | d5faf89f-3641-4be1-8d43-35504f12fe8d | 2026-04-22 | Warnings | M012 |
| Multi-Symptom Cold childrens | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | WALMART INC. | 5ee5eb75-fc56-42a1-bf2c-b9c10ea8bfd4 | 2026-04-22 | Warnings | M012 |
| good sense nasal | OXYMETAZOLINE HYDROCHLORIDE | L. Perrigo Company | 95f23049-e523-4c59-904c-b8e9ae82602c | 2026-04-22 | Warnings | M012 |
| Mucinex Childrens FreeFrom Multi-Symptom Cold and Stuffy Nose | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Reckitt Benckiser LLC | c07dad99-87b0-419b-9230-7c22a77ecf9e | 2026-04-21 | Warnings | M012 |
| Cough and Cold HBP | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Valu Merchandisers Company | 83db90da-9155-4f6a-8209-44c87d14b696 | 2026-04-21 | Warnings | M012 |
| Pain, Headache and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 613a2516-fc61-4bb4-bd44-ca6004548193 | 2026-04-21 | Warnings | M012 |
| Dr. Simi Allergy Relief | DIPHENHYDRAMINE HCL | Farmacias De Similares TX LLC | 4fe8bbe3-13c9-5458-e063-6294a90a9064 | 2026-04-20 | Warnings | M012 |
| Cold and Flu Day and Night, Severe | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | ARMY AND AIR FORCE EXCHANGE SERVICE | 58d722ef-db67-44ac-a295-dd10e1f5ca1d | 2026-04-20 | Warnings | M012 |
| Loratadine 10mg | LORATADINE | BETTER LIVING BRANDS, LLC | 46d615dd-45d5-2dfc-e063-6394a90a5d42 | 2026-04-18 | Warnings | M012 |
| Multi-Symptom Cold Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Valu Merchandisers Company | d0f896a6-5637-45ef-bf60-b343cbcdcf7e | 2026-04-17 | Warnings | M012 |
| MUCUS RELIEF | GUAIFENESIN | Bryant Ranch Prepack | 9ed5611f-4e1d-4f71-b430-a2a949bf7fe5 | 2026-04-17 | Warnings | M012 |
| Multi-Symptom Cold | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Valu Merchandisers Company | bf3158af-89ab-4b7c-9f39-0f316fbe9056 | 2026-04-17 | Warnings | M012 |
| MUCUS RELIEF | GUAIFENESIN | Bryant Ranch Prepack | 761825bc-f835-4947-bfa0-2940f1dff5fb | 2026-04-17 | Warnings | M012 |
| equate cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | WALMART INC. | e83d14cc-9b90-40ce-a00a-2702d8a8968f | 2026-04-17 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 995868 | codeine phosphate 10 MG / guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 88d0994c-4270-4408-8837-bd97510b2118 | 11 |
| 995868 | codeine phosphate 2 MG/ML / guaifenesin 20 MG/ML Oral Solution | SCD | 88d0994c-4270-4408-8837-bd97510b2118 | 11 |
| 995868 | codeine phosphate 10 MG / guaifenesin 100 MG per 5 ML Oral Solution | SY | 88d0994c-4270-4408-8837-bd97510b2118 | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0121-1550-00 | 00121155000 | 10 TRAY in 1 CASE (0121-1550-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10) | 10 tray | 2006-10-01 | 0000-00-00 | No | No | Current |
| 0121-1550-10 | 00121155010 | 10 mL in 1 CUP, UNIT-DOSE | 10 ml | Historical | ||||
| 0121-1550-40 | 00121155040 | 4 TRAY in 1 CASE (0121-1550-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10) | 4 tray | 2024-01-10 | No | No | Current |