Guaifenesin STRAWBERRY-BANANA FLAVOR
- Product NDC
- 71800-059
- 11-digit product format
- 718000059
- Labeler code
- 71800
- Product ID
- 71800-059_37de006a-e717-a4e5-e063-6394a90abd8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GUAIFENESIN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Innovida Pharmaeutique Corporation
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-16
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- 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
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 STRAWBERRY-BANANA FLAVOR
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 100 mg/5mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 495W7451VQ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 310604 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 4fe95224-f543-4dbb-9445-8cca122b48c8 | Product name | 1 | 20150609 |
| e8718272-64cb-4436-969b-176c3067c8f4 | Product name | 1 | 20150609 |
| 106ff02a-57e1-4c4c-a307-fd582ff4e311 | Product name | 1 | 20150212 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71800-059-19 | Guaifenesin STRAWBERRY-BANANA FLAVOR | 119 mL in 1 TUBE | LIQUID | 119 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71800-059-19 | ML - Milliliter | 71800-059 | d3fa3ffd-d057-44a7-b7b8-f8d657a3803c | 1 | 2026-04-20 |
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 |
|---|---|---|---|---|---|---|
| Akin Cough Formula DM | DEXTROMETHORPHAN, GUAIFENESIN | Southern Sales & Service, Inc. | 1f2f9b4c-ecf0-4ff6-861a-063f8a9ef74a | 2023-11-29 | Warnings | M012 |
| diphenhydramine hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Simpex Pharma Pvt. Ltd | 82771f6a-8b3d-4ffa-8b35-09c2faf3582c | 2023-11-29 | Warnings | M012 |
| SIMPEX Guaifenesin | GUAIFENESIN | Simpex Pharma Pvt. Ltd | 1594f9d6-0c48-42bf-b76b-d621f215179a | 2023-11-29 | Warnings | M012 |
| Stona | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Sato Pharmaceutical Co., Ltd. | 8b89f50d-88f8-4773-92ea-5ada61766056 | 2023-11-28 | Warnings | M012 |
| Stona | DEXTROMETHORPHAN HYDROBROMIDE | Sato Pharmaceutical Co., Ltd. | 1ccc9e56-32a4-450f-8412-5814b6aef285 | 2023-11-28 | Warnings | M012 |
| Neo-Synephrine Maximum | PHENYLEPHRINE HYDROCHLORIDE | BF ASCHER AND CO INC | ab8682a4-1f66-6709-e053-2995a90a8b4a | 2023-11-16 | Warnings | M012 |
| Neo-Synephrine Regular | PHENYLEPHRINE HYDROCHLORIDE | BF ASCHER AND CO INC | ab860c10-b8cf-3f92-e053-2a95a90a7317 | 2023-11-16 | Warnings | M012 |
| Neo-Synephrine Mild | PHENYLEPHRINE HYDROCHLORIDE | BF ASCHER AND CO INC | 9b8e9162-e4da-14d9-e053-2995a90a2269 | 2023-11-16 | Warnings | M012 |
| Universal Vaporizing Chest Rub | MENTHOL AND CAMPHOR AND EUCALYPTUS | Universal Distribution Center LLC | b1d25572-da21-408d-aab3-3a0741dfff12 | 2023-11-16 | Warnings | M012 |
| Daytime Cold and Flu Severe, Caseys 4goog | ACETAMINOPHEN, PHENYLEPHRINE, DEXTROMETHORPHAN HBR, GUAIFENESIN TABLET, FILM COATED | Lil' Drug Store Products, Inc. | 0334259d-587e-b2d5-e063-6394a90a3e56 | 2023-11-14 | Warnings | M012 |
| Stona Cough | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | Sato Pharmaceutical Co., Ltd. | 0b638db4-5ed3-4665-abcd-f95e677adbd8 | 2023-11-12 | Warnings | M012 |
| Tylenol Sinus Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Jones Healthcare Group - Packaging Services, Inc | 6c90b415-4c5f-49e5-beb6-4cf225797b21 | 2023-11-06 | Warnings | M012 |
| Tylenol Cold Plus Flu Severe Severe | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Jones Healthcare Group - Packaging Services, Inc | 8b8582c0-8aef-482f-9738-2f1d4e325d64 | 2023-11-06 | Warnings | M012 |
| Cold and Flu Severe Daytime/Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DOXYLAMINE SUCCINATE | Topco Associates LLC | 27ade5f8-2003-4dc6-9244-42676791e1f8 | 2023-11-06 | Warnings | M012 |
| Benadryl Allergy Ultratab | DIPHENHYDRAMINE HYDROCHLORIDE | Jones Healthcare Group - Packaging Services, Inc | ec2070df-8a8a-4cd1-8830-62655433fb3b | 2023-11-05 | Warnings | M012 |
| Daytime Nighttime Ultra Concentrated Cold and Flu | DAYTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR AND NIGHTTIME - ACETAMINOPHEN, DEXTROMETHROPHAN HBR, DOXYLAMINE SUCCINATE | TARGET CORPORATION | 093eed84-79b1-7914-e063-6394a90a37af | 2023-11-03 | Warnings | M012 |
| Cough Drops | MENTHOL | Topco Associates LLC | eff68377-2273-6c6c-e053-2995a90a36b2 | 2023-11-03 | Warnings | M012 |
| Sugar Free Cough Drops | MENTHOL | Topco Associates LLC | 096bbcaa-fce1-0fc2-e063-6294a90ad597 | 2023-11-03 | Warnings | M012 |
| TopCare Nite Time SEVERE Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Topco Associates LLC | adc8edf5-ebbe-4d94-9018-aa0dbe118112 | 2023-11-03 | Warnings | M012 |
| MUCOSA | GUAIFENESIN | TIME CAP LABORATORIES,INC | d34ef2e8-adc2-48e5-a572-e354937daec6 | 2023-11-02 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310604 | guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 20 MG/ML Oral Solution | SCD | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Solution | SY | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Syrup | SY | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 200 MG per 10 ML Oral Solution | SY | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 300 MG per 15 ML Oral Solution | SY | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
| 310604 | guaifenesin 400 MG per 20 ML Oral Solution | SY | 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 71800-059-19 | 71800005919 | 119 mL in 1 TUBE (71800-059-19) | 119 ml | 2025-06-16 | No | No | Current |