NDC 47046-153-01 - Hemorrhoid Anesthetic
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
- 47046-153
- Requested NDC
- 47046-153-01
- Package NDCs from labels
- 47046-153-01, 47046-153-02
- Manufacturer
- Anicare Pharmaceuticals Pvt. Ltd
- Effective date
- 2020-12-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hemorrhoid Anesthetic - Anicare Pharmaceuticals Pvt. Ltd | Anicare Pharmaceuticals Pvt. Ltd | 2020-12-13 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 47046-153-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-9a7e-a426-e053-dadaa90af4c2 | Hemorrhoid Anesthetic Ointment |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 47046-153-01 | Hemorrhoid Anesthetic | 28 g in 1 TUBE | OINTMENT | 28 | 1 | |
| 47046-153-02 | Hemorrhoid Anesthetic | 1 in 1 CARTON | OINTMENT | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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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| Baza Clear | PETROLATUM | Coloplast Corp | 69d9f456-1a35-4146-8366-c0285648a172 | 2026-03-27 | Warnings | 4T6H12BN9U |
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| DAYTIME SEVERE COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | CVS HEALTH CORP | 2ba90b91-2e35-4701-e063-6294a90a7554 | 2026-03-24 | Warnings | 04JA59TNSJ |
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| Cold and Head Congestion Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | DOLGENCORP, LLC | ed28bfa9-3768-4f42-ae5e-1c527b4456d1 | 2026-03-24 | Warnings | 04JA59TNSJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.