HEMORRHOID MASTER- lidocaine, phenylephrine hcl ointment 
Clinical Resolution Laboratory, Inc.

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Active Ingredients

Lidocaine 4.00%

Phenylephrine HCl 0.25%

Directions

■ Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Children under 12 years of age: consult a doctor.

■ For External Use: Apply externally to the affected area up to 4 times daily.

■ For Intrarectal use: Attach applicator to tube. Lubricate applicator well, then gently insert applicator into the rectum. Apply to the affected area up to 4 times daily.

Warnings:For external and/ or intrarectal use only.

■ If condition worsens or does not improve within 7 days, consult a doctor.

■ Do not exceed the recommended daily dosage unless directed by a doctor.

■ In case of bleeding, consult a doctor promptly.

■ Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

■ Do not use this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.

■ Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression.

■ Do not use this product with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult a doctor promptly.

Uses

■ For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders and anorectal inflammation.

■ For the temporary relief of pain, burning and soreness.

■ Temporarily shrinks hemorrhoidal tissue.

■ Temporarily reduces the swelling associated with irritation in hemorrhoids and other anorectal disorders.

■ Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Children under 12 years of age: consult a doctor.

■ For External Use: Apply externally to the affected area up to 4 times daily.

■ For Intrarectal use: Attach applicator to tube. Lubricate applicator well, then gently insert applicator into the rectum. Apply to the affected area up to 4 times daily.

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Ascorbic Acid, Ascorbyl Palmitate, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetearyl Alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Cholesterol, Diisopropyl Sebacate, Dimethyl Isosorbide, Dodecane, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Hexylene Glycol, Hydrocortisone, Isododecane, Isopropyl Myristate, Lecithin, Mentha Piperita (Peppermint) Oil, Microcrystalline Wax, Mineral Oil, Octyldodecanol, Panax Ginseng Root Extract, PEG-8 Dimethicone, Petrolatum, Phenoxyethanol, Phospholipids, Polyethylene, Propylene Glycol, Punica Granatum Extract, Pyridoxine HCl, Retinyl Palmitate, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Stearic Acid, Tocopheryl Acetate, Triethoxycaprylylsilane, Water, Zea Mays (Corn) Oil, Zinc Oxide

Purpose

Local Anesthetic

Vasoconstrictor

Other Information

■ Keep away from direct sunlight or heat.

■ Store at room temperature 15°-30°C (59°-86°F).

■ Keep out of reach of children.

■ In case of accidental overdose or ingestion, call a doctor or poison control center immediately.

■ Do not use this product if seal is broken or missing.

HM Master 4%

Packaging Label

HEMORRHOID MASTER 
lidocaine, phenylephrine hcl ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63742-045
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 mg  in 1 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
PETROLATUM (UNII: 4T6H12BN9U)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
MINERAL OIL (UNII: T5L8T28FGP)  
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
HYDROCORTISONE (UNII: WI4X0X7BPJ)  
WATER (UNII: 059QF0KO0R)  
ZEA MAYS (CORN) OIL (UNII: 8470G57WFM)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)  
PANAX GINSENG ROOT (UNII: CUQ3A77YXI)  
SILICA (UNII: ETJ7Z6XBU4)  
CHOLECALCIFEROL, (5E)- (UNII: W28SLM7V6D)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
DODECANE (UNII: 11A386X1QH)  
ETHOXYDIGLYCOL (UNII: A1A1I8X02B)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
POLYETHYLENE (UNII: UG00KM4WR7)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
RETINYL PALMITATE (UNII: 1D1K0N0VVC)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
ISODODECANE (UNII: A8289P68Y2)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
POMEGRANATE (UNII: 56687D1Z4D)  
PYRIDOXINE HCL (UNII: 68Y4CF58BV)  
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CHAMOMILE (UNII: FGL3685T2X)  
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL (UNII: 65UEH262IS)  
CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
Product Characteristics
Colorwhite (Yellowish White) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63742-045-0145 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product11/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01511/01/2019
Labeler - Clinical Resolution Laboratory, Inc. (825047942)
Registrant - Clinical Resolution Laboratory, Inc. (825047942)
Establishment
NameAddressID/FEIBusiness Operations
Clinical Resolution Laboratory, Inc.825047942manufacture(63742-045)

Revised: 6/2025
Document Id: 36caf20d-116b-f86a-e063-6294a90a7b62
Set id: 36caf20d-116a-f86a-e063-6294a90a7b62
Version: 1
Effective Time: 20250604
 
Clinical Resolution Laboratory, Inc.