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
- 2025-11-26
- 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. | 2025-11-26 | 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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| Caldesene Medicated Protecting | CORNSTARCH AND ZINC OXIDE | Insight Pharmaceuticals LLC | ffc92a0f-a7cf-4a46-b2f1-089df2bbb96b | 2026-04-22 | Warnings | SOI2LOH54Z |
| Hydrocortisone 1% | HYDROCORTISONE | Preferred Pharmaceuticals Inc. | e0f46445-64c5-4f5d-90b0-3fa07ed7d1b4 | 2026-04-22 | Warnings | WI4X0X7BPJ |
| Hydravex | HYDRAVEX | Oncora Pharma, LLC | 1da8a263-354a-4ab1-90b4-cc2ecba7c2f6 | 2026-04-22 | Warnings, Adverse reactions | WI4X0X7BPJ |
| Pure Eyes Sterile Eyes | NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN | SAMSON PHARMACEUTICAL | c0234e82-211f-4731-ac48-12db13b16e8a | 2026-04-21 | Warnings | PDC6A3C0OX |
| Broad Spectrum SPF45 | ZINC OXIDE, OCTINOXATE | Drmtlgy, LLC | 0445ee5f-45a8-4fd5-ae4d-62f66e6f0be8 | 2026-04-21 | Warnings | SOI2LOH54Z |
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| Freaks of Nature Mineral Sunscreen | ZINC OXIDE MINERAL SUNSCREEN | Empack Spraytech Inc. | 4ffdb1c6-b2c6-628f-e063-6394a90a2769 | 2026-04-21 | Warnings | SOI2LOH54Z |
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| Vitavera | VITAVERA | Oncora Pharma, LLC | 058b1921-21da-49d9-b9c1-3f5636087aea | 2026-04-21 | Warnings, Adverse reactions | PQ6CK8PD0R 9E8X80D2L0 |
| Oraqix | LIDOCAINE AND PRILOCAINE | Dentsply Pharmaceutical | b501d239-923b-48b2-82ed-6c5c253a67e2 | 2026-04-21 | Warnings, Adverse reactions | 98PI200987 |
| KT Pain Relief Cream Magnesium with Arnica and 4% Lidocaine | KT PAIN RELIEF CREAM MAGNESIUM WITH ARNICA AND 4% LIDOCAINE ROLLON | Clarion Brands LLC | 4f82993c-ebc4-5787-e063-6294a90a12d6 | 2026-04-20 | Warnings | 98PI200987 |
| Rhtalgorism Delay Sprays for Men | PANAX GINSENG ROOT EXTRACT 7% | Guangdong Meizhiyuan Biotechnology Co., Ltd. | 4fe00413-0938-2c82-e063-6294a90a3b1f | 2026-04-20 | Warnings | CUQ3A77YXI |
| Lidothol ES Patch | LIDOTHOL ES PATCH | Direct_Rx | 4fe72fca-9689-fff4-e063-6394a90a3ad2 | 2026-04-20 | Warnings, Adverse reactions | 98PI200987 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.