NDC 70942-357-07 - Dr Butlers Hemorrhoid and Fissure PF
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
- 70942-357
- Requested NDC
- 70942-357-07
- Package NDCs from labels
- 70942-357-00, 70942-357-01, 70942-357-07, 70942-357-75, 70942-357-06, 70942-357-12, 70942-357-05, 70942-357-15
- Manufacturer
- Beyond Health P.A.
- Effective date
- 2026-10-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dr Butler Hemorrhoid & Fissure Ointment PF | Beyond Health P.A. | 2026-10-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70942-357-00 | Dr Butlers Hemorrhoid and Fissure PF | 28 g in 1 TUBE | OINTMENT | 28 | 5 | |
| 70942-357-01 | Dr Butlers Hemorrhoid and Fissure PF | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 70942-357-05 | Dr Butlers Hemorrhoid and Fissure PF | 42.5 g in 1 TUBE | OINTMENT | 42.5 | 5 | |
| 70942-357-06 | Dr Butlers Hemorrhoid and Fissure PF | 2 g in 1 PACKET | OINTMENT | 2 | 5 | |
| 70942-357-07 | Dr Butlers Hemorrhoid and Fissure PF | 21.3 g in 1 TUBE | OINTMENT | 21.3 | 5 | |
| 70942-357-12 | Dr Butlers Hemorrhoid and Fissure PF | 12 in 1 CARTON | OINTMENT | 12 | 5 | |
| 70942-357-15 | Dr Butlers Hemorrhoid and Fissure PF | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 70942-357-75 | Dr Butlers Hemorrhoid and Fissure PF | 1 in 1 CARTON | OINTMENT | 1 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70942-357-07 | GM - Gram | 70942-357 | 33bcdb8c-dc7c-460c-88a9-a08b3eb6ecfc | 1 | 2025-11-13 |
| 70942-357-75 | GM - Gram | 70942-357 | 3b213a17-51e1-483f-ad34-8d8d9712ebff | 1 | 2025-09-12 |
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.
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| TKTALKER NUMBING | NUMBING | Shenzhen Shandian Jingling Technology Co., Ltd. | 3d7e6757-f183-2a68-e063-6294a90ae4ca | 2025-08-29 | Warnings | 98PI200987 |
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| Dolce and Gabbana Everlast Foundation SPF 20 32W Medium Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | ba99edea-bf68-4118-8bb7-ea40322db46a | 2025-08-29 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Everlast Foundation SPF 20 34W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 3a239897-9850-417f-8c00-e810a52540c1 | 2025-08-29 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Everlast Foundation SPF 20 36N Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | c495afc3-6486-4652-b743-958f28eccaca | 2025-08-29 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Everlast Foundation SPF 20 35W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 5440ed13-b07e-4c81-a407-d9ac68eaa483 | 2025-08-29 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Everlast Foundation SPF 20 37W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 9b2c4567-fde7-4b76-9988-b2cba2d3747e | 2025-08-29 | Warnings | SOI2LOH54Z |
| else. | LIDOCAINE | Else Co. | 3d6c7b10-ed03-bbde-e063-6294a90ae92f | 2025-08-28 | Warnings | 98PI200987 |
| Sterile Water | WATER INJECTION | Henry Schein, Inc. | 3501952b-b556-4d5e-b81b-5c35ff87b475 | 2025-08-28 | Warnings, Adverse reactions | 059QF0KO0R |
| Multivitamin with Fluoride | SODIUM FLUORIDE | WINDER LABORATORIES, LLC | a10ff759-eba7-414b-bb98-f17fbb6e6b57 | 2025-08-27 | Warnings, Adverse reactions | PQ6CK8PD0R 1C6V77QF41 |
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| Sun Bum 30 Mineral Tinted Sunscreen Face | TITANIUM DIOXIDE, ZINC OXIDE | Sun Bum, LLC | 3a290aad-7f40-cb10-e063-6394a90a2e69 | 2025-08-27 | Warnings | SOI2LOH54Z |
| Sinus Relief Pressure and Pain | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | Kroger Company | 98de5cff-3ff5-49b0-bef9-5b9ebb86491e | 2025-08-27 | Warnings | 04JA59TNSJ |
| Nighttime SEVERE | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | H E B | 0a178114-0748-4a92-9b60-a7a0a8b72287 | 2025-08-26 | Warnings | 04JA59TNSJ |
| Sun Bum 50 Mineral Sunscreen Face Stick | ZINC OXIDE | Sun Bum, LLC | 3d48d467-4b6b-c477-e063-6294a90a5a0d | 2025-08-26 | Warnings | SOI2LOH54Z |
| PAPATUI Facial Moisturizer Broad Spectrum SPF 30 | ZINC OXIDE | PAPATUI, LLC | 3d4ab3a5-a29b-bdd9-e063-6294a90a542c | 2025-08-26 | Warnings | SOI2LOH54Z |
| naked TURTLE 30 | ZINC OXIDE | NAKED TURTLE SUNSCREEN LLC | 65f1570a-6156-40e6-a792-e0707607dc2f | 2025-08-26 | Warnings | SOI2LOH54Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.