tucks triple relief hemorrhoidal

Generic: white petrolatum, glycerin, pramoxine hydrochloride, and phenylephrine hydrochloride

Labeler: blistex inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tucks triple relief hemorrhoidal
Generic Name white petrolatum, glycerin, pramoxine hydrochloride, and phenylephrine hydrochloride
Labeler blistex inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

glycerin 15 g/100g, phenylephrine hydrochloride .25 g/100g, pramoxine hydrochloride 1 g/100g, white petrolatum 16 g/100g

Manufacturer
Blistex Inc.

Identifiers & Regulatory

Product NDC 10157-2126
Product ID 10157-2126_19acdb94-4437-4eaf-aa16-0bef186d9f8a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M015
Listing Expiration 2026-12-31
Marketing Start 2025-01-06

Pharmacologic Class

Established (EPC)
non-standardized chemical allergen [epc]
Chemical Structure
allergens [cs] glycerol [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 101572126
Hyphenated Format 10157-2126

Supplemental Identifiers

RxCUI
2701523
UNII
PDC6A3C0OX 04JA59TNSJ 88AYB867L5 B6E5W8RQJ4
NUI
N0000185370 N0000175629 N0000184306 N0000185001 M0000728 M0009417

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tucks triple relief hemorrhoidal (source: ndc)
Generic Name white petrolatum, glycerin, pramoxine hydrochloride, and phenylephrine hydrochloride (source: ndc)
Application Number M015 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 15 g/100g
  • .25 g/100g
  • 1 g/100g
  • 16 g/100g
source: ndc
Packaging
  • 1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR
source: ndc

Packages (1)

Ingredients (4)

glycerin (15 g/100g) phenylephrine hydrochloride (.25 g/100g) pramoxine hydrochloride (1 g/100g) white petrolatum (16 g/100g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "19acdb94-4437-4eaf-aa16-0bef186d9f8a", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "unii": ["PDC6A3C0OX", "04JA59TNSJ", "88AYB867L5", "B6E5W8RQJ4"], "rxcui": ["2701523"], "spl_set_id": ["bf892e90-2d9b-4fa0-8ee4-8a2736be6c30"], "pharm_class_cs": ["Allergens [CS]", "Glycerol [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Blistex Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1)  / 26 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "10157-2126-1", "marketing_start_date": "20250106"}], "brand_name": "Tucks Triple Relief Hemorrhoidal", "product_id": "10157-2126_19acdb94-4437-4eaf-aa16-0bef186d9f8a", "dosage_form": "CREAM", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Allergens [CS]", "Cell-mediated Immunity [PE]", "Glycerol [CS]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Chemical Allergen [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "10157-2126", "generic_name": "WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Blistex Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tucks Triple Relief Hemorrhoidal", "active_ingredients": [{"name": "GLYCERIN", "strength": "15 g/100g"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": ".25 g/100g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100g"}, {"name": "WHITE PETROLATUM", "strength": "16 g/100g"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250106", "listing_expiration_date": "20261231"}