tucks triple relief hemorrhoidal
Generic: white petrolatum, glycerin, pramoxine hydrochloride, and phenylephrine hydrochloride
Labeler: blistex inc.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
Active Ingredients
glycerin 15 g/100g, phenylephrine hydrochloride .25 g/100g, pramoxine hydrochloride 1 g/100g, white petrolatum 16 g/100g
Manufacturer
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)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
101572126
Hyphenated Format
10157-2126
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 15 g/100g
- .25 g/100g
- 1 g/100g
- 16 g/100g
Packaging
- 1 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR
Packages (1)
Ingredients (4)
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"}