Label: HEALSURE HEMORRHOID FISSURE- lidocaine 4%, phenylephrine hcl 0.25%, hemorrhoid fissure ointment
- NDC Code(s): 84010-107-01
- Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 6, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
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Do not use
Do not put this product into the rectum.
Ask a doctor before use if you have allergies to any of the components of this product, difficulty in urination due to enlargement of the prostate gland, diabetes, heart disease, high blood pressure, thyroid disease, or presently taking a prescription for high blood pressure or depression.
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
Children under 12 years of age should consult their pediatrician. Adults: apply to affected area up to 3 times daily.Clean affected area with mild soap and warm water, rinse thoroughly, and then 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. - Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HEALSURE HEMORRHOID FISSURE
lidocaine 4%, phenylephrine hcl 0.25%, hemorrhoid fissure ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84010-107 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 HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 0.25 g in 100 g Inactive Ingredients Ingredient Name Strength BORNEOL (UNII: M89NIB437X) GLYCERIN (UNII: PDC6A3C0OX) THYMOL (UNII: 3J50XA376E) ALOE (UNII: V5VD430YW9) CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84010-107-01 20 g in 1 TUBE; Type 0: Not a Combination Product 05/06/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/06/2025 Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056) Establishment Name Address ID/FEI Business Operations Jiangxi Hemei Pharmaceutical Co., Ltd 724892056 manufacture(84010-107)

