NDC 70000-0696-01 - Leader Adult Tussin Mucus and Chest Congestion 541
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70000-0696
- Requested NDC
- 70000-0696-01
- Package NDCs from labels
- 70000-0696-1, 70000-0696-2, 70000-0696-01
- Manufacturer
- CARDINAL HEALTH 110, LLC. DBA LEADER | Guardian Drug Company
- Effective date
- 2024-09-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Guaifenesin - CARDINAL HEALTH 110, LLC. DBA LEADER | Guardian Drug Company | CARDINAL HEALTH 110, LLC. DBA LEADER | Guardian Drug Company | 2024-09-20 | Human OTC Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70000-0696-1 | Leader Adult Tussin Mucus and Chest Congestion 541 | 118 mL in 1 BOTTLE | LIQUID | 118 | 1 | |
| 70000-0696-1 | Leader Adult Tussin Mucus and Chest Congestion 541 | 1 in 1 CARTON | LIQUID | 1 | 1 | |
| 70000-0696-2 | Leader Adult Tussin Mucus and Chest Congestion 541 | 237 mL in 1 BOTTLE | LIQUID | 237 | 1 | |
| 70000-0696-2 | Leader Adult Tussin Mucus and Chest Congestion 541 | 1 in 1 CARTON | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70000-0696 | LEADER ADULT TUSSIN MUCUS AND CHEST CONGESTION 541 (GUAIFENESIN) LIQUID [CARDINAL HEALTH 110, LLC. DBA LEADER] | 1 | Current NDC, 4 package rows | 20240922_d7fae410-9c1c-4231-9fde-2c51ad3d7e95.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0696-1 | ML - Milliliter | 70000-0696 | 44710a7e-f55d-4b69-9471-e0b5957d7215 | 1 | 2025-10-14 |
| 70000-0696-2 | ML - Milliliter | 70000-0696 | d2e80e9a-1023-4243-b96f-ba44776f0aed | 1 | 2025-05-14 |
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 |
|---|---|---|---|---|---|---|
| Pain Reliever PM Extra strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Walgreens | 54cbbc5f-908b-47b2-b37f-3646354d3568 | 2026-08-27 | Warnings | M012 |
| Maximum Strength Mucus Relief | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Hyvee Inc | 4e578c7a-88d4-e4cd-e063-6394a90aac44 | 2026-08-27 | Warnings | M012 495W7451VQ |
| MUCUS RELIEF | GUAIFENESIN | Geri-Care Pharmaceuticals, Corp | 5afb242f-fac9-dc81-e063-6394a90a8448 | 2026-08-27 | Warnings | M012 495W7451VQ |
| daytime cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE | Amazon.com Services LLC | 6de619d3-0ab0-43e7-8dac-7bbd5368ac65 | 2026-08-27 | Warnings | M012 |
| Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum Strength | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, ACETAMINOPHEN, DIPHENHYDRAMINE HCI | Walgreens | 366ddac8-9e8a-41bd-a7f7-48213485a5f8 | 2026-08-27 | Warnings | M012 |
| Nighttime Cold and Flu Maximum Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI | Walgreens | 37896933-3ed3-457f-8a32-ee0d784a19e8 | 2026-08-27 | Warnings | M012 |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | Amazon.com Services LLC | 298e9164-e378-4b39-a944-bfc8f8baa4de | 2026-08-27 | Warnings | M012 |
| DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength | DAYTIME ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, NIGHTTIME ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI | Walgreens | 3b4b3b04-eff9-4e06-8b37-f6729671d07f | 2026-08-27 | Warnings | M012 |
| Careland Lidocaine Plus Menthol Pain Relieving | LIDOCAINE, MENTHOL | Planet (Anhui) Pharmaceutical Co., Ltd | 0f928b5b-60f5-4a45-a409-c601eb330487 | 2026-08-26 | Warnings | L7T10EIP3A |
| PARCHE CALIENTE | CAPSAICINA AND MENTOL | DW SUPPORT LLC | 59f2708e-295a-ccb3-e063-6394a90ad395 | 2026-08-26 | Warnings | L7T10EIP3A |
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Daytime Cold and Flu mini Softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | dfb0fe2e-b0c7-409a-bd1a-fd12485665ba | 2026-08-26 | Warnings | M012 |
| Nighttime Severe Cold and Flu Maximum Strength mini softgels | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Shield Pharmaceuticals Corp | 70c5517d-be4e-4317-b4f4-df660c71c699 | 2026-08-26 | Warnings | M012 |
| Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Meijer Distribution, Inc. | c1f9ec75-7eb2-405c-8cdc-097cbf2cf87d | 2026-08-26 | Warnings | M012 495W7451VQ |
| robafen dm | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN | Preferred Pharmaceuticals Inc. | 5b2fd5ce-56ab-491a-81b9-44e35a5d2316 | 2026-08-26 | Warnings | 495W7451VQ |
| Childrens TYLENOL COLD plus COUGH plus RUNNY NOSE | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, AND DEXTROMETHORPHAN HYDROBROMIDE | Kenvue Brands LLC | 5b95905e-b729-4caf-921a-fc4ef815289c | 2026-08-25 | Warnings | M012 |
| Kreain Nature Soothing Cooling | KREAIN NATURE SOOTHING COOLING | WANWANG INC | 59e046de-2be7-26bd-e063-6394a90a4b31 | 2026-08-25 | Warnings | L7T10EIP3A |
| mucus dm | DEXTROMETHORPHAN HBR, GUAIFENESIN | HyVee Inc | 6bce66d6-e76a-4273-aff9-7ee6adc18980 | 2026-08-25 | Warnings | 495W7451VQ |
| good neighbor pharmacy mucus dm | DEXTROMETHORPHAN HBR, GUAIFENESIN | Amerisource Bergen | f7925a6b-7029-4389-bf1b-8c0f5e79b950 | 2026-08-25 | Warnings | 495W7451VQ |
| Allergy Relief | DIPHENHYDRAMINE HCL | Wal-Mart Stores Inc | c88e93d4-66b6-4327-b9e5-0e0a95a18d66 | 2026-08-25 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.