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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Alka-Seltzer Plus Maximum Strength Day Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 5172dc01-4e7f-3307-e054-00144ff8d46c | 2025-12-04 | Warnings | 04JA59TNSJ |
| Alka-Seltzer Plus Maximum Strength Cold and Cough Liquid Gels | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 20ae92d9-fbc6-5b7a-e063-6294a90a15c3 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Alka-Seltzer Plus Maximum Strength Night Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 51dca689-e4a0-5526-e054-00144ff88e88 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 6f2d18f6-935f-9215-e053-2a91aa0aedd3 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Alka-Seltzer Plus Maximum Strength Severe Sinus, Allergy and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 5213ca7f-5a78-6471-e054-00144ff88e88 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Alka-Seltzer Plus Maximum Strength Night Cold and Flu PowerMax Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | 6f7ba256-ed14-5fe0-e053-2a91aa0aacc1 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Solbar Zinc SPF38 | SOLBAR ZINC SPF38 | Person and Covey | fac62a2f-92ee-4afd-9999-bc5011159e43 | 2025-12-04 | Warnings | SOI2LOH54Z |
| Menthol and Zinc Oxide | MENTHOL AND ZINC OXIDE | Marlex Pharmaceuticals, Inc. | c24e2dab-cab4-38f4-e053-2995a90aabae | 2025-12-04 | Warnings | M015 SOI2LOH54Z |
| elf Sun Boss Gloss SPF 25 Sunscreen Pink Me Girl | ZINC OXIDE | e.l.f. Cosmetics, Inc. | 6c316ce4-c2f6-4633-a789-e786d0f76abd | 2025-12-04 | Warnings | SOI2LOH54Z |
| Binda Botanicals Baby and Kids Sunscreen SPF50 | ZINC OXIDE SUNSCREEN | VEGANIC SKN LIMITED | 452b9b7d-4049-b483-e063-6394a90a5358 | 2025-12-04 | Warnings | SOI2LOH54Z |
| BINDA Face and Body Sunscreen SPF50 | ZINC OXIDE SUNSCREEN | VEGANIC SKN LIMITED | 386f5013-430c-e07f-e063-6394a90a32a8 | 2025-12-04 | Warnings | SOI2LOH54Z |
| GENCONTUSS | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | KRAMER NOVIS | 69d16d25-b09b-430e-8e01-0962d840dc21 | 2025-12-04 | Warnings | 04JA59TNSJ |
| Nasal Decongestant PE | PHENYLEPHRINE HCL | H E B | 7c04ab14-af28-4598-90ef-56ac11902c7d | 2025-12-04 | Warnings | 04JA59TNSJ |
| Desgen Pediatric | DEXTROMETHORPHAN HBR, GUIAFENESIN, PHENYLEPHRINE HCL | Kramer Novis | 12425c1b-8bdc-446b-83dd-95e05a4d9b8c | 2025-12-04 | Warnings | 04JA59TNSJ |
| Presgen B | DEXTROMETHORPHAN HYDROBROMIDE, BROMPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE | KRAMER NOVIS | 5befa829-32bd-4978-8a0e-1d6513ff37a4 | 2025-12-03 | Warnings | 04JA59TNSJ |
| Health One Pain Relief Cream with Lidocaine 4% | PAIN RELIEF CREAM WITH LIDOCAINE 4% | ONE2ZEE LIMITED LIABILITY COMPANY | 46a2276f-9da0-4e41-92f0-b17c302c7222 | 2025-12-03 | Warnings | 98PI200987 |
| TUSSLIN | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | Kramer Novis | 987e19a5-032f-44e9-b4c7-8a764d502695 | 2025-12-03 | Warnings | 04JA59TNSJ |
| Lidocaine Patch | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 38767081-7011-6602-e063-6394a90a2784 | 2025-12-03 | Warnings | 98PI200987 |
| 4% Lidocaine Maximum Strength Pain Relief | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 3e5a5165-a773-0501-e063-6294a90ae2f4 | 2025-12-03 | Warnings | 98PI200987 |
| UNIVERSAL PURE PETROLEUM | WHITE PETROLEUM | Universal Distribution Center LLC | 6bc34bbe-e324-48f4-b6df-dd508b19c2e2 | 2025-12-03 | Warnings | 4T6H12BN9U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.