Label: LIPOSOMAL HEMORRHOID MASTER- lidocaine hcl 4%, phenylephrine hcl 0.25% ointment
- NDC Code(s): 84735-008-01
- Packager: Hengyang Chuangjiujia Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 12, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
-
INDICATIONS & USAGE
Uses. Forthe temporany relief of local and anorectal iching and discomfot asociated with anoreclal isorders and anorectalimammation.
Forthe temporany reief of pain,buring and sorenes.
Temporarily shrinks hemorthoidal tisue, Temporarily reduces the sweling associated with iritation in hemorthoids and other anorectal disorders.
- WARNINGS
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DO NOT USE
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.
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Petrolatum
Aloe Barbadensis Leaf Extract
Glycerin
Mineral Oil
Chamomilla Recutita (Matricaria) Flower Extract
Tocopherol
Ascorbic Acid
Pyridoxine HCl
Ginseng Extract
Propylene Glycol
Sodium Hyaluronate
Polysorbate 80
Panthenol
Allantoin
Phenoxyethanol
Ethylhexylglycerin
Carbomer
Triethanolamine
Water - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIPOSOMAL HEMORRHOID MASTER
lidocaine hcl 4%, phenylephrine hcl 0.25% ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84735-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 4 g in 100 g PHENYLEPHRINE (UNII: 1WS297W6MV) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 0.25 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM HYALURONATE (UNII: YSE9PPT4TH) PYRIDOXINE HCL (UNII: 68Y4CF58BV) CHAMOMILE (UNII: FGL3685T2X) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ASCORBIC ACID (UNII: PQ6CK8PD0R) TRIETHANOLAMINE (UNII: 9O3K93S3TK) ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) MINERAL OIL (UNII: T5L8T28FGP) TOCOPHEROL (UNII: R0ZB2556P8) DEXPANTHENOL (UNII: 1O6C93RI7Z) ALLANTOIN (UNII: 344S277G0Z) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CARBOMER (UNII: 0A5MM307FC) PETROLATUM (UNII: 4T6H12BN9U) ASIAN GINSENG (UNII: CUQ3A77YXI) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84735-008-01 50 g in 1 TUBE; Type 0: Not a Combination Product 05/12/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/12/2025 Labeler - Hengyang Chuangjiujia Trading Co., Ltd. (977292157) Establishment Name Address ID/FEI Business Operations Hengyang Chuangjiujia Trading Co., Ltd. 977292157 manufacture(84735-008)

