Label: HEMORRHOID MASTER- lidocaine, phenylephrine ointment
- NDC Code(s): 72654-002-01
- Packager: Ebanel Laboratories, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 26, 2023
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- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredient
- Uses
-
Warnings
For external and or intrarectal use only.
Stop use and ask a doctor
- If condition worsens or does not improve within 7 days.
- in case of bleeding.
- if allergic reaction to product occurs. If the symptoms being treated does not subside or if redness. irritation, swelling, pain, or other sympoms develop or increase.
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.
- with an applicator if the introduction of the applicator into the rectum causes additional pain. Consult doctor promptly.
-
Directions
Adults: Apply to the affected area up to 3 times dialy.
- Children under 12 years of age: consult a doctor.
- When practical, clean affected area with mild soap and warm water and rinse thoroughly. Gently dry (patting or blotting) with tissue or soft cloth before use.
- To use dispensing cap, attach it to tube, lubricate well, then gently insert part way into anus and squeeze tube to deliver medication. Thoroughly cleanse dispensing cap after use with mild soap and warm water and rinse thoroughly.
- For Intrarectal Use:
-
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, 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, Polysorbate 80, Propylene Glycol, Punica Granatum Extract, Pyridoxine HCl, Retinyl Palmitate, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica, Stearic Acid, Tocopheryl Acetate, Triethoxycaprylylsilane, Zea Mays (Corn) Oil, Zinc Oxide.
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
HEMORRHOID MASTER
lidocaine, phenylephrine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72654-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g PHENYLEPHRINE (UNII: 1WS297W6MV) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ASCORBIC ACID (UNII: PQ6CK8PD0R) ASCORBYL PALMITATE (UNII: QN83US2B0N) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SAFFLOWER OIL (UNII: 65UEH262IS) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CHAMOMILE (UNII: FGL3685T2X) CHOLECALCIFEROL (UNII: 1C6V77QF41) CHOLESTEROL (UNII: 97C5T2UQ7J) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) DODECANE (UNII: 11A386X1QH) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) HYDROCORTISONE (UNII: WI4X0X7BPJ) ISODODECANE (UNII: A8289P68Y2) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PEPPERMINT OIL (UNII: AV092KU4JH) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) MINERAL OIL (UNII: T5L8T28FGP) OCTYLDODECANOL (UNII: 461N1O614Y) ASIAN GINSENG (UNII: CUQ3A77YXI) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PETROLATUM (UNII: 4T6H12BN9U) PHENOXYETHANOL (UNII: HIE492ZZ3T) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CORN (UNII: 0N8672707O) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72654-002-01 45 g in 1 TUBE; Type 0: Not a Combination Product 11/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/01/2019 Labeler - Ebanel Laboratories, Inc (079352161)
