Haemorrhoidal Pain Relief
Haemorrhoidal Pain Relief is an FDA drug label for the active ingredient ANORECTAL CREAM manufactured by NeilMed Pharmaceuticals Inc administered by RECTAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260615.
- Generic name
- ANORECTAL CREAM
- Manufacturer
- NeilMed Pharmaceuticals Inc
- Product type
- HUMAN OTC DRUG
- Route
- RECTAL
- Dosage form
- N/A
- NDC
- 13709-358
- Application
- M015
- Label effective
- 20260615
About this product
Haemorrhoidal Pain Relief is an FDA-registered drug product whose active ingredient is ANORECTAL CREAM. It is labelled by NeilMed Pharmaceuticals Inc taken by rectal and marketed as a human otc drug product. Identifiers on file: NDC 13709-358, application M015, label effective 20260615. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ANORECTAL CREAM are most often described in connection with: temporarily relieves, itching due, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses temporarily relieves pain and itching due to anorectal disorders. Uses
Dosage & Administration
Directions Clean the area with mild soap and warm water and rinse thoroughly. Gently dry the area by patting or blotting with toilet tissue or a soft cloth before applying to the affected area up to six (6) times per day. Recommended for use by adults and children 12 years and older. Directions
Warnings
Warnings When Using this Product Avoid contact with eyes do not exceed recommended dosage unless directed by a doctor Warnings
Recall and safety notices
1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0569-2024 | SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12 Hour Relief, 0.5 fl oz (15 ml) bottle, Manufactured by NeilMed Pharmaceuticals Inc, 602 Aviation Blvd, Santa Rosa, CA 95403 877-477-8633; NDC 13709-325-01; UPC 7 05928 09001 9. | Neilmed Pharmaceuticals Inc | Class III | Ongoing | 20240703 |
Frequently asked questions
What is Haemorrhoidal Pain Relief used for?
Uses temporarily relieves pain and itching due to anorectal disorders. Uses
Who makes Haemorrhoidal Pain Relief?
NeilMed Pharmaceuticals Inc is the labeler of record for Haemorrhoidal Pain Relief.
What form does Haemorrhoidal Pain Relief come in?
administered by rectal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Haemorrhoidal Pain Relief prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Haemorrhoidal Pain Relief been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.