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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Epionce Daily Shield Tinted SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Episciences, Inc. | 3d1e2921-cba9-4446-e054-00144ff8d46c | 2026-06-04 | Warnings | SOI2LOH54Z |
| GNP Calamine Topical Suspension | CALAMINE 8% AND ZINC OXIDE 8% | Amerisource Bergen | 777b0e66-1bce-4483-9dad-c46796fd6f23 | 2026-06-04 | Warnings | SOI2LOH54Z |
| GNP Caldyphen | CALAMINE AND PRAMOXINE HYDROCHLORIDE | Amerisource Bergen | 515c58d7-0dc4-45e7-9155-e5270a16290e | 2026-06-04 | Warnings | SOI2LOH54Z |
| Mineral Glowscreen Soft-Radiance Drops Golden Hour | ZINC OXIDE | Supergoop LLC | 1f1be2a7-af96-d73d-e063-6394a90acc1a | 2026-06-04 | Warnings | SOI2LOH54Z |
| Derma E Sun Drops SPF 30 | ZINC OXIDE | derma e | 76c29f24-e0d9-4235-b278-96e609bc58db | 2026-06-04 | Warnings | SOI2LOH54Z |
| Lidocaine | LIDOCAINE | Sun Pharmaceutical Industries, Inc. | 5eb2c62f-5352-41d7-bd66-c65b1988a9ab | 2026-06-03 | Warnings, Adverse reactions | 98PI200987 |
| ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB | ZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDE | HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED | 5354af18-50c4-5fba-e063-6394a90ace39 | 2026-06-03 | Warnings | SOI2LOH54Z |
| Stye Eye Relief Serum | HIPPOPHAE RHAMNOIDES SEED OIL , CALENDULA OFFICINALIS FLOWER , PERSEA GRATISSIMA (AVOCADO) OIL | Guangxi Keyun E-commerce Co., Ltd. | 535516ac-2279-7f92-e063-6294a90a04ae | 2026-06-03 | Warnings | P0M7O4Y7YD |
| Severe Congestion and Cough | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Walgreen Company | b0c1d635-0f85-433a-b479-51c68d259faa | 2026-06-03 | Warnings | 04JA59TNSJ |
| Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM | HyVee Inc | b867f691-7a13-4659-b664-06aa36899310 | 2026-06-03 | Warnings | M015 4T6H12BN9U PDC6A3C0OX 04JA59TNSJ |
| Vitalux | MULTIVITAMIN | PureTek Corporation | 52d5eee7-8146-cc62-e063-6394a90a8c3f | 2026-06-02 | Boxed warning, Adverse reactions | PQ6CK8PD0R SOI2LOH54Z 1C6V77QF41 |
| ATOMY BB SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | b0cd27ee-4917-4800-bcdf-c6e14b28c1d1 | 2026-06-02 | Warnings | SOI2LOH54Z |
| Atomy Sunscreen White Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | ad0b9091-a990-45bf-93f4-d886be1bbffe | 2026-06-02 | Warnings | SOI2LOH54Z |
| Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | 994d5680-284e-4faf-a29b-4d28f8d46e8f | 2026-06-02 | Warnings | SOI2LOH54Z |
| BLDG Active Skin Repair Sun Stick Performance Sunscreen | ZINC OXIDE | Innovacyn, Inc. | a751fc1d-5ee4-4ecc-8ade-2568d91890c4 | 2026-06-02 | Warnings | SOI2LOH54Z |
| Biofreeze Ultraflex | LIDOCAINE | Reckitt Benckiser LLC | 2655974b-a67d-9f07-e063-6294a90a54e8 | 2026-06-02 | Warnings | 98PI200987 |
| Biofreeze Ultraflex Plus | LIDOCAINE, MENTHOL | Reckitt Benckiser LLC | 401e1843-e9a6-fda9-e063-6294a90a3073 | 2026-06-02 | Warnings | 98PI200987 |
| ALKA SELTZER COLD Cold and Flu plus Congestion Severe Fast Hot Liquid Night | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 5349dbde-730c-610f-e063-6394a90a952a | 2026-06-02 | Warnings | 04JA59TNSJ |
| Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 | ZINC OXIDE, TITANIUM DIOXIDE | Private Label Skin Care | a8d60212-18a7-42af-8bb3-bfcff7690a49 | 2026-06-02 | Warnings | SOI2LOH54Z |
| The Mineral Melt SPF30 | ZINC OXIDE, TITANIUM DIOXIDE | Dune Suncare Inc. | 2114fc3b-c8ce-45d2-8a82-4dc54f0adaf3 | 2026-06-02 | Warnings | SOI2LOH54Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.