NDC 10157-2126 – Tucks Triple Relief Hemorrhoidal
White Petrolatum 16 g/100g; Glycerin 15 g/100g; Pramoxine Hydrochloride 1 g/100g; Phenylephrine Hydrochloride .25 g/100g · Cream · Topical
Product NDC10157-2126
Product details
- Brand name
- Tucks Triple Relief Hemorrhoidal
- Generic name
- WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, and PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- Blistex Inc.
- Dosage form
- Cream
- Route
- Topical
- Marketing category
- OTC MONOGRAPH DRUG · M015
- Marketed since
- January 6, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Non-Standardized Chemical Allergen; alpha-1 Adrenergic Agonist
Active ingredients
- White Petrolatum 16 g/100g
- Glycerin 15 g/100g
- Pramoxine Hydrochloride 1 g/100g
- Phenylephrine Hydrochloride .25 g/100g
Uses, dosage, side effects and warnings for Tucks Triple Relief Hemorrhoidal →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 10157-2126-1 | 1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR | Jan 6, 2025 |