Hemorrhoidal Pain Relief
- Product NDC
- 13709-334
- 11-digit product format
- 137090334
- Labeler code
- 13709
- Product ID
- 13709-334_374d89b6-9306-9adf-e063-6394a90adb32
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hemorrhoidal Pain Relief Ointment
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Neilmed Pharmaceuticals Inc.
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-11
- Substance
- MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 140; 749; 2.5 mg/g; mg/g; mg/g
- Pharmacologic classes
- Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hemorrhoidal Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINERAL OIL | 140 mg/g |
| PETROLATUM | 749 mg/g |
| PHENYLEPHRINE HYDROCHLORIDE | 2.5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T5L8T28FGP, 4T6H12BN9U, 04JA59TNSJ |
| Rxcui | 1372298 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 13709-334-01 | Hemorrhoidal Pain Relief | 57 g in 1 TUBE | OINTMENT | 57 | | 1 |
| 13709-334-01 | Hemorrhoidal Pain Relief | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 13709-334-01 | 13709033401 | 1 TUBE in 1 CARTON (13709-334-01) / 57 g in 1 TUBE | 1 tube | 2025-06-11 | No | No | Current |