ProCure Hemorrhoidal
- Product NDC
- 55681-021
- 11-digit product format
- 556810021
- Labeler code
- 55681
- Product ID
- 55681-021_37cdd72a-2001-148c-e063-6394a90af289
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mineral Oil, Petrolatum, Phenylephrine HCl
- Dosage form
- OINTMENT
- Route
- RECTAL; TOPICAL
- Labeler
- Twin Med LLC
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-16
- Substance
- MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 14; 74.9; .25 g/100g; g/100g; g/100g
- 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
- ProCure Hemorrhoidal
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINERAL OIL | 14 g/100g |
| PETROLATUM | 74.9 g/100g |
| PHENYLEPHRINE HYDROCHLORIDE | .25 g/100g |
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 |
|---|
| 55681-021-02 | ProCure Hemorrhoidal | 56.6 g in 1 TUBE, WITH APPLICATOR | OINTMENT | 56.6 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-021-02 | 55681002102 | 56.6 g in 1 TUBE, WITH APPLICATOR (55681-021-02) | 56.6 g | 2025-06-16 | No | No | Current |