NDC 75920-0464-01 - Blowfish
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
- 75920-0464
- Requested NDC
- 75920-0464-01
- Package NDCs from labels
- 75920-0464-1, 75920-0464-8, 75920-0464-2, 75920-0464-4, 75920-0464-6, 75920-0464-5, 75920-0464-7, 75920-0464-01
- Manufacturer
- Rally Labs LLC | Tower Laboratories Ltd
- Effective date
- 2025-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Blowfish - Rally Labs LLC | Tower Laboratories Ltd | Rally Labs LLC | Tower Laboratories Ltd | 2025-12-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75920-0464-1 | Blowfish | 2 in 1 BOX | TABLET, EFFERVESCENT | 2 | 10 | |
| 75920-0464-2 | Blowfish | 20 in 1 BAG | TABLET, EFFERVESCENT | 20 | 10 | |
| 75920-0464-4 | Blowfish | 40 in 1 BAG | TABLET, EFFERVESCENT | 40 | 10 | |
| 75920-0464-5 | Blowfish | 20 in 1 BOX | TABLET, EFFERVESCENT | 20 | 10 | |
| 75920-0464-6 | Blowfish | 4 in 1 BOX | TABLET, EFFERVESCENT | 4 | 10 | |
| 75920-0464-7 | Blowfish | 20 in 1 BOX | TABLET, EFFERVESCENT | 20 | 10 | |
| 75920-0464-8 | Blowfish | 12 in 1 BOX | TABLET, EFFERVESCENT | 12 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 75920-0464 | BLOWFISH (ASPIRIN, CAFFEINE) TABLET, EFFERVESCENT [RALLY LABS LLC] | 9 | Current NDC, Legacy NDC, 7 package rows | 20241218_0d3798bc-04ef-584e-821b-7aa76036b7d1.zip |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Xenleta | LEFAMULIN ACETATE | Meitheal Pharmaceuticals Inc. | eb972ea8-7502-422e-84bb-66cb8e93ca06 | 2026-07-22 | Warnings, Adverse reactions | XF417D3PSL |
| Childrens Acetaminophen | ACETAMINOPHEN | Cardinal Health 107, LLC | 7562f4e4-54fa-488c-a199-48ad2632e2a1 | 2026-07-21 | Warnings | M013 |
| Medline | ACETAMINOPHEN | Medline Industries, LP | 4b1d7243-b943-4e2b-e063-6294a90a2c4e | 2026-07-20 | Warnings | M013 |
| Stool Softener Laxative | DOCUSATE SODIUM | Bryant Ranch Prepack | deca083b-5c72-40fa-9021-b74028426a5a | 2026-07-20 | Warnings | F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | Cardinal Health 107, LLC | fc5e82b6-e25c-4686-9781-2205819685f5 | 2026-07-20 | Warnings | F05Q2T2JA0 |
| Butalbital, Acetaminophen, Caffeine | BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE | HAWAII REPACK, INC. | ab882f60-394c-4d4f-95f4-6b9d6d6b3193 | 2026-07-17 | Boxed warning, Warnings, Adverse reactions | 3G6A5W338E |
| Acetaminophen | ACETAMINOPHEN | LEADER/ Cardinal Health 110, Inc. | 7c342ae6-5de6-5c2f-e053-2a91aa0a3f0d | 2026-07-16 | Warnings | M013 |
| Rapidol 500 Extra Strength | ACETAMINOPHEN | Pharmadel LLC | 1d9fa7ec-a509-28b2-e063-6294a90a7831 | 2026-07-16 | Warnings | M013 |
| stool softener | DOCUSATE SODIUM | Amazon.com Services LLC | 4f83953e-3779-43b7-a5c6-7442a0675d9b | 2026-07-16 | Warnings | F05Q2T2JA0 |
| Stool Softener Extra Strength | DOCUSATE SODIUM | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 183576bd-c252-471b-8797-32cac5b0329c | 2026-07-16 | Warnings | F05Q2T2JA0 |
| equate pain relief | ACETAMINOPHEN | WALMART INC. | 2f9b2550-5476-49ae-b741-54416a40bc29 | 2026-07-16 | Warnings | M013 |
| Stool Softener | DOCUSATE SODIUM | Walgreens | 3f9d54d9-a9d5-40ff-a8a2-431997b58999 | 2026-07-16 | Warnings | F05Q2T2JA0 |
| Pain Relief PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | HyVee Inc | 4f45a750-1220-4a81-801e-bf08c9d117d6 | 2026-07-16 | Warnings | M013 |
| Stool Softener Laxative | DOCUSATE SODIUM | Walgreens | 7174021b-bdc0-4fd3-90e7-3904980033c4 | 2026-07-16 | Warnings | F05Q2T2JA0 |
| Acetaminophen Extra Strength | ACETAMINOPHEN | Dr. Reddy's Laboratories Inc. | 9d34abc2-3a9a-b68f-80d4-4ede1eb1e45f | 2026-07-15 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Family Dollar, Inc. | 3f182571-3212-eb29-e063-6294a90a9fa0 | 2026-07-15 | Warnings | M013 |
| Stool Softener | DOCUSATE SODIUM | STRATEGIC SOURCING SERVICES LLC | ff2179bd-cc76-9ee9-e053-6294a90a01c9 | 2026-07-15 | Warnings | F05Q2T2JA0 |
| Quality Choice Effervescent Cold Relief - Plus | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE | Chain Drug Marketing Association | 1f93fe6d-ee21-e323-e063-6394a90a61bf | 2026-07-15 | Warnings | R16CO5Y76E |
| Quality Choice Effervescent Cold Relief - Orange | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE | Chain Drug Marketing Association | 1f93c815-63c7-bfe0-e063-6394a90ab4a5 | 2026-07-15 | Warnings | R16CO5Y76E |
| FEVIA Constipation Control | DOCUSATE SODIUM | VIVUNT PHARMA LLC | 4b21ca11-b81f-402c-e063-6394a90a3acb | 2026-07-15 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.