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 |
|---|---|---|---|---|---|---|
| e.l.f. Hydrating Camo CC Cream SPF30 Fair 100 W | HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE | e.l.f. Cosmetics, Inc. | 3fa7ef54-2c4d-9883-e063-6294a90a8d88 | 2025-09-17 | Warnings | SOI2LOH54Z |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Family Dollar (FAMILY WELLNESS) | 5d7466b4-fdb7-432b-880d-e7aa4a4acbda | 2025-09-17 | Warnings | 04JA59TNSJ |
| CVS SPF 50 Face Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | CVS | 26a69a47-947a-a478-e063-6394a90aa468 | 2025-09-16 | Warnings | SOI2LOH54Z |
| DayTime Cold Flu Non Drowsy | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | Harris Teeter, LLC | 67beb9f6-4e0a-4f7b-b50a-4bcd3a01354f | 2025-09-16 | Warnings | 04JA59TNSJ |
| DOMETUSS | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Domel Laboratories | 3ebfc62f-27f6-48b2-9bae-bdefbd1d05fe | 2025-09-16 | Warnings | 04JA59TNSJ |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | FSA Store Inc. (Caring Mills) | e69ef8dc-09d2-46de-aebf-ba735f4cc7ea | 2025-09-16 | Warnings | 04JA59TNSJ |
| SkinSuit TM 3 in 1 Moisturizer SPF 50 | ZINC OXIDE | Skin Authority LLC | 5eb27be9-9e80-4f4a-b193-b918d831555d | 2025-09-15 | Warnings | SOI2LOH54Z |
| Sun and Honey Tallow Sunscreen SPF 30 | ZINC OXIDE | Amara Ventures | 3eda8a70-7c9e-e920-e063-6394a90a85a2 | 2025-09-15 | Warnings | SOI2LOH54Z |
| Perikabiven | DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE | Fresenius Kabi USA, LLC | c2eb5522-8572-45f4-869d-42f9fd251bb6 | 2025-09-15 | Warnings, Adverse reactions | JNJ23Q2COM |
| REFRESH OPTIVE Drops | CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN | Allergan, Inc. | 80275190-d717-40ea-905b-5c8fbe986eac | 2025-09-15 | Warnings | PDC6A3C0OX |
| Refresh Relieva PF Xtra | CARBOXYMETHYLCELLULOSE SODIUM AND GLYCERIN | Allergan, Inc. | b51b8a75-8faa-430f-8f7e-ee58d3d13f2e | 2025-09-15 | Warnings | PDC6A3C0OX |
| Refresh Relieva | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Allergan, Inc. | 6b984fa2-4187-45ef-b7d3-15e720abc667 | 2025-09-15 | Warnings | PDC6A3C0OX |
| I.C. Industrial Sunscreen | ZINC OXIDE, OCTINOXATE, OXYBENZONE, AND OCTISALATE | R & R Lotion, Inc | b89d687a-7b36-4643-9817-765d4710ca60 | 2025-09-15 | Warnings | SOI2LOH54Z |
| Lidocaine-Pain-Relief-Patch | LIDOCAINE-PAIN-RELIEF-PATCH | Henan Enokon Medical Instrument Co., Ltd. | 3ecfa867-50f6-d98a-e063-6394a90aefa0 | 2025-09-14 | Warnings | 98PI200987 |
| Meijer Hydrocortsione Cream | HYDROCORTSIONE CREAM 1% | Meijer Distribution Inc. | 1cbddb7e-f2e3-0951-e063-6394a90a3d37 | 2025-09-12 | Warnings | WI4X0X7BPJ |
| Dolce and Gabbana Blueberry Nutri Tint SPF 20 36N Deep | ZINC OXIDE | DOLCE & GABBANA BEAUTY S.R.L. | 2d05659c-57d2-4faf-ab67-1b8d68945aed | 2025-09-12 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Blueberry Nutri Tint SPF 20 37W Deep | ZINC OXIDE | DOLCE & GABBANA BEAUTY S.R.L. | 5ff2b9e4-a778-4667-8c3c-3561317b374a | 2025-09-12 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Blueberry Nutri Tint SPF 20 39N Deep | ZINC OXIDE | DOLCE & GABBANA BEAUTY S.R.L. | bc4f909f-3e2c-4fd7-a129-3c2fac8259f0 | 2025-09-12 | Warnings | SOI2LOH54Z |
| Dolce and Gabbana Blueberry Nutri Tint SPF 20 40C Deep | ZINC OXIDE | DOLCE & GABBANA BEAUTY S.R.L. | 2dd9a30a-2cde-44c0-9350-3aeab9f7091b | 2025-09-12 | Warnings | SOI2LOH54Z |
| Dry eye relief | POLYETHYLENE GLYCOL AND PROPYLENE GLYCOL | CARDINAL HEALTH 110, LLC. DBA LEADER | f8da3af5-9172-4023-be82-0fd5bd891616 | 2025-09-12 | Warnings | 6DC9Q167V3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.