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 |
|---|---|---|---|---|---|---|
| Sinus Congestion and Pain Daytime | ACETAMINOPHEN AND PHENYLEPHRINE HCL | United Natural Foods, Inc. dba UNFI | f3fc270a-92fc-46d5-b187-44e875c3abb9 | 2026-02-09 | Warnings | 04JA59TNSJ |
| Sinus Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | L.N.K. International, Inc. | d5c8b248-6d82-4eac-881c-0b9d0a0de8f1 | 2026-02-09 | Warnings | 04JA59TNSJ |
| ASSIELF NUMBING Topical Anorectal | LIDOCAINE | Shenzhen Yuanbang International Logistics Co., Ltd | 4a5cb477-57ef-2a1d-e063-6394a90ac9ed | 2026-02-08 | Warnings | 98PI200987 |
| Lidocaine Pain Relieve Gel-Patch | PAIN RELIEVE GEL-PATCH | Henan Kangdi Medical Devices Co., Ltd | 1e31b950-e990-e255-e063-6394a90a7d23 | 2026-02-07 | Warnings | 98PI200987 |
| NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Goddess Glow | ZINC OXIDE SUNSCREEN | Bentley Laboratories, LLC | bb86322d-ff30-4a54-97b5-1be275067146 | 2026-02-06 | Warnings | SOI2LOH54Z |
| Lidocaine Pain Relief Gel-Patch | LIDOCAINE | Shenzhen Wankelai E-commerce Co., Ltd. | 4a22562b-601e-97d7-e063-6394a90a5bca | 2026-02-06 | Warnings | 98PI200987 |
| hydrocortisone | HYDROCORTISONE | Sportpharm LLC | ee64ad1e-78db-4553-a3cf-b539b770fa26 | 2026-02-06 | Warnings | WI4X0X7BPJ |
| Pain Relief Gel-Patch | LIDOCAINE 4% | Sportpharm LLC | 1dd022b9-88ae-4737-88cc-fdb0ce0a83a3 | 2026-02-06 | Warnings | 98PI200987 |
| Hampton Sun SPF 50 Mineral | ZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00% | S&C Hampton Sun LLC | d6c33436-042e-44e8-8b55-98be6e246879 | 2026-02-06 | Warnings | SOI2LOH54Z |
| Petrolatum | WHITE PETROLATUM | Retail Business Services, LLC | bf0c9494-0138-4346-9348-e235ca4d9e58 | 2026-02-06 | Warnings, Adverse reactions | 4T6H12BN9U |
| Advanced Healing | PETROLATUM | Retail Business Services, LLC | 6e9121c8-5eb9-4d0b-86c5-b892e14bdab8 | 2026-02-06 | Warnings | 4T6H12BN9U |
| Camphor plus Lidocaine Pain Relief | CAMPHOR, LIDOCAINE | Veridian Healthcare | 4a2b73a8-c10c-85f9-e063-6294a90ac52c | 2026-02-06 | Warnings | 98PI200987 |
| Petrolatum | WHITE PETROLATUM | Retail Business Services, LLC | bf73c618-ed2f-4468-a51f-ff61c7b1f506 | 2026-02-06 | Warnings, Adverse reactions | 4T6H12BN9U |
| Mineral Oil | MINERAL OIL | Retail Business Services, LLC | b0abcdf9-c226-424f-8970-c2135708c6c8 | 2026-02-06 | Warnings, Adverse reactions | T5L8T28FGP |
| Petroleum | WHITE PETROLATUM | Salado Sales Inc. | f973e3a5-3b45-4842-99ce-dff676ae1f96 | 2026-02-06 | Warnings, Adverse reactions | 4T6H12BN9U |
| NUDESCREEN DEWY ILLUMINATING GLOW SPF 30 - Sunkissed Glow | ZINC OXIDE SUNSCREEN | Bentley Laboratories, LLC | bf1a237b-b27e-4c55-8ded-e348240a5b9a | 2026-02-06 | Warnings | SOI2LOH54Z |
| Severe Allergy And Sinus Headache Maximum Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL | CVS Pharmacy | b3c744b8-aa93-505d-f8cf-07995da4283d | 2026-02-06 | Warnings | 04JA59TNSJ |
| Severe Sinus Daytime, Non-Drowsy | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | Walgreen Company | cc0dc951-5024-4517-9d38-a01699407e7e | 2026-02-06 | Warnings | 04JA59TNSJ |
| SEYTU Body Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | c411e9a6-b2ea-446b-a886-b92c61736e6c | 2026-02-05 | Warnings | SOI2LOH54Z |
| SEYTU Facial Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Omnilife USA, Inc. | 96fd37fb-c3ff-413f-b2c8-50754f320ecc | 2026-02-05 | Warnings | SOI2LOH54Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.