FDA.reportPublic FDA data

Tucks Triple Relief Hemorrhoidal

Product NDC
10157-2126
11-digit product format
101572126
Labeler code
10157
Product ID
10157-2126_19acdb94-4437-4eaf-aa16-0bef186d9f8a
Type
HUMAN OTC DRUG
Nonproprietary name
WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, and PHENYLEPHRINE HYDROCHLORIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
Blistex Inc.
Application
M015
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-06
Substance
GLYCERIN; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE; WHITE PETROLATUM
Active strength
15; .25; 1; 16 g/100g; g/100g; g/100g; g/100g
Pharmacologic classes
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]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Tucks Triple Relief Hemorrhoidal
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GLYCERIN15 g/100g
PHENYLEPHRINE HYDROCHLORIDE.25 g/100g
PRAMOXINE HYDROCHLORIDE1 g/100g
WHITE PETROLATUM16 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiPDC6A3C0OX, 04JA59TNSJ, 88AYB867L5, B6E5W8RQJ4
Rxcui2701523

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814Product name320150910
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-2126-1Tucks Triple Relief Hemorrhoidal26 g in 1 TUBE, WITH APPLICATORCREAM261
10157-2126-1Tucks Triple Relief Hemorrhoidal1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-2126TUCKS TRIPLE RELIEF HEMORRHOIDAL (WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE) CREAM [BLISTEX INC.]1Current NDC, 2 package rows20250108_bf892e90-2d9b-4fa0-8ee4-8a2736be6c30.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2701523glycerin 15 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 16 % Rectal CreamPSNbf892e90-2d9b-4fa0-8ee4-8a2736be6c301
2701523glycerin 150 MG/ML / petrolatum 160 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal CreamSCDbf892e90-2d9b-4fa0-8ee4-8a2736be6c301
2701523glycerin 15 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 16 % Rectal CreamSYbf892e90-2d9b-4fa0-8ee4-8a2736be6c301

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
10157-2126-1101572126011 TUBE, WITH APPLICATOR in 1 CARTON (10157-2126-1) / 26 g in 1 TUBE, WITH APPLICATOR2025-01-06NoNoHistorical