Guaifenesin
- Product NDC
- 81033-102
- 11-digit product format
- 810330102
- Labeler code
- 81033
- Product ID
- 81033-102_316ac9e6-8d03-f55a-e063-6294a90a8540
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- KESIN PHARMA CORPORATION
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-20
- 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
- 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 |
|---|---|
| 365c01b7-a197-4876-85fc-42204f787e3a | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 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 |
| 6084a4f4-5437-c9a5-caec-5361ee075a59 | Product name | 1 | 20140508 |
| 90c5639a-61b0-88d6-ddcf-21888e94869a | Product name | 1 | 20140508 |
| 9514609b-a2a9-f8ec-6ba6-3f8e5ee89877 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-102-05 | Guaifenesin | 5 mL in 1 CUP, UNIT-DOSE | LIQUID | 5 | 7 | |
| 81033-102-10 | Guaifenesin | 10 mL in 1 CUP, UNIT-DOSE | LIQUID | 10 | 7 | |
| 81033-102-51 | Guaifenesin | 50 in 1 CARTON | LIQUID | 50 | 7 | |
| 81033-102-52 | Guaifenesin | 50 in 1 CARTON | LIQUID | 50 | 7 | |
| 81033-102-16 | Guaifenesin | 473 mL in 1 BOTTLE | LIQUID | 473 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-102-05 | ML - Milliliter | 81033-102 | c04493a2-a5df-4be5-86e1-38cd698bbd63 | 1 | 2024-03-12 |
| 81033-102-10 | ML - Milliliter | 81033-102 | a990cc84-2678-4699-8dca-ec8808a024a4 | 1 | 2024-04-05 |
| 81033-102-16 | ML - Milliliter | 81033-102 | 7a1f8916-cb71-4e4c-a447-b4f532f27ea3 | 1 | 2025-06-13 |
| 81033-102-51 | ML - Milliliter | 81033-102 | 118824ef-231f-4404-85a9-9e31242703de | 1 | 2024-01-04 |
| 81033-102-52 | ML - Milliliter | 81033-102 | 0be6c67c-993a-4d6d-9ecc-515e876c5d39 | 1 | 2024-01-04 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81033-102 | GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION] | 7 | Current NDC, 4 package rows | 20250331_365c01b7-a197-4876-85fc-42204f787e3a.zip |
| 81033-102 | GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION] | 1 | Current NDC, 1 package rows | 20250406_31b8ad0a-3637-03db-e063-6394a90acdc3.zip |
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 |
|---|---|---|---|---|---|---|
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | 7-ELEVEN | 2f3c43dd-175f-722e-e063-6294a90acff9 | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | 7-ELEVEN | 2f3c3c65-4178-6304-e063-6294a90a51fa | 2025-02-28 | Warnings | M012 |
| Menthol Cough Drops Creamy Strawberry Flavor | MENTHOL AND PECTIN | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efbffd7-bbdd-c5f5-e063-6294a90a15f0 | 2025-02-25 | Warnings | M012 |
| Menthol Cough Drops Honey Vanilla Flavor | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 2efc46c9-a421-1998-e063-6394a90aeb64 | 2025-02-25 | Warnings | M012 |
| Redicare Cough Drops Cherry Flavored | CHERRY FLAVORED MENTHOL COUGH DROPS | Redicare LLC | 2efeaafa-ee96-37ee-e063-6394a90a9a4b | 2025-02-25 | Warnings | M012 |
| Childrens Allergy | DIPHENHYDRAMINE HCL | Genexa Inc. | e880b8d7-61c3-41cc-e053-2995a90aaaeb | 2025-02-20 | Warnings | M012 |
| Gencare-Nasal Decongestant PE | PHENYLEPHRINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 596ec923-56a0-4b6e-a69c-8d740feb75a2 | 2025-02-20 | Warnings | M012 |
| Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 2-pack | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Kenvue Brands LLC | 77a2dc96-73ee-4ca2-b1fe-406995802606 | 2025-02-19 | Warnings | M012 |
| nasal decongestant | OXYMETAZOLINE HYDROCHLORIDE | Safeway | f1d0edd5-fe58-4de0-98f4-07fb24bd0ac2 | 2025-02-19 | Warnings | M012 |
| Coricidin HBP Cold and Flu | ACETAMINOPHEN AND CHLORPHENIRAMINE MALEATE | Bayer HealthCare LLC. | 763a5334-a741-4678-9947-603776622450 | 2025-02-18 | Warnings | M012 |
| Sof Skin Vaporizing Chest Rub and Cough Suppressant | MENTHOL AND CAMPHOR AND EUCALYPTUS OIL | Viny Health and Beauty Inc | 46ae16a4-b8a7-44de-ae1a-9bb503c15ea0 | 2025-02-18 | Warnings | M012 |
| Pain Reliever PM | ACETAMINOPHEN DIPHENHYDRAMINE HCL | QUALITY CHOICE (Chain Drug Marketing Association) | 4897d1df-4fb3-46e2-bbf0-847e964dca0a | 2025-02-18 | Warnings | M012 |
| meijer EXTRA STRENGTH Pain Relief PM Caplet | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | Meijer, Inc. | 1bee7e4f-1813-1bdf-e063-6294a90a6a32 | 2025-02-17 | Warnings | M012 |
| ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAILFENESIN,PHENLYEPHRINE HCL | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAILFENESIN,PHENLYEPHRINE HCL | Kroger Company | a24f09d9-60f1-853a-e053-2a95a90ae1fa | 2025-02-15 | Warnings | M012 |
| MAXIMUM STRENGTH COLD AND FLU | ACETAMINOPHEN,DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | FAMILY DOLLAR SERVICES | a7343bea-53cc-4621-e053-2a95a90a2a5f | 2025-02-15 | Warnings | M012 |
| MAXIMUM STRENGTH DAY-NIGHT COLD AND FLU FORMULA | ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL | FAMILY DOLLAR | aa8f6dd0-d19f-0c10-e053-2a95a90a1e8a | 2025-02-15 | Warnings | M012 |
| MAXIMUM STRENGHT DAY COLD AND FLU FORMULA | ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL | FAMILY DOLLAR | aa8ebccf-6813-2dca-e053-2a95a90a032b | 2025-02-15 | Warnings | M012 |
| MAXIMUM STRENTH NIGHT COLD AND FLU FORMULA | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | FAMILY DOLLAR | aa8f0465-1595-0b0f-e053-2a95a90a0081 | 2025-02-15 | Warnings | M012 |
| DAYTIME SEVERE COLD AND FLU | ACETAMINOPHEN, PHENYLEPHRINE HCL, DEXTROMETHORPHAN HBR, GUAIFENESIN | KROGER COMPANY | 9bb7aaf0-6698-9a5c-e053-2a95a90a097c | 2025-02-14 | Warnings | M012 |
| Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | H-E-B | db432947-fe02-79b2-e053-2a95a90af4a9 | 2025-02-14 | Warnings | M012 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310604 | guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 20 MG/ML Oral Solution | SCD | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Solution | SY | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Syrup | SY | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 200 MG per 10 ML Oral Solution | SY | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 300 MG per 15 ML Oral Solution | SY | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaifenesin 400 MG per 20 ML Oral Solution | SY | 365c01b7-a197-4876-85fc-42204f787e3a | 7 |
| 310604 | guaiFENesin 100 MG in 5 mL Oral Solution | PSN | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 20 MG/ML Oral Solution | SCD | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Solution | SY | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 100 MG per 5 ML Oral Syrup | SY | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 200 MG per 10 ML Oral Solution | SY | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 300 MG per 15 ML Oral Solution | SY | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
| 310604 | guaifenesin 400 MG per 20 ML Oral Solution | SY | 31b8ad0a-3637-03db-e063-6394a90acdc3 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 81033-102-05 | 81033010205 | 5 mL in 1 CUP, UNIT-DOSE | 5 ml | Historical | |||
| 81033-102-10 | 81033010210 | 10 mL in 1 CUP, UNIT-DOSE | 10 ml | Historical | |||
| 81033-102-16 | 81033010216 | 473 mL in 1 BOTTLE (81033-102-16) | 473 ml | 2025-04-01 | No | No | Current |
| 81033-102-51 | 81033010251 | 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05) | 2023-11-20 | No | No | Current | |
| 81033-102-52 | 81033010252 | 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10) | 2023-11-20 | No | No | Current |