Label: THE PHARMA C COMPANY TRIPLE ACTION HEMORRHOIDAL PADS- witch hazel, lidocaine, phenylephrine hydrochloride cloth
- NDC Code(s): 55239-459-00
- Packager: Kleen Test Products Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 8, 2024
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- Drug Facts
- Active ingredients
- Uses
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Warnings
For external use only.
Ask a doctor before use if you have
• heart disease • high blood pressure • thyroid disease • diabetes • difficulty in urination due to enlargement of the prostate gland
Ask a doctor before use if you are
presently taking a prescription drug for high blood pressure or depression
When using this product
- do not use more than directed unless told to do so by a doctor
- do not put directly in the rectum by using fingers or mechanical device
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Directions
Adults:
- when practical, clean 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 applying
- apply externally to the affected area up to 4 times daily
- after application, discard pad and wash hands
Children under 12 years of age: ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
THE PHARMA C COMPANY TRIPLE ACTION HEMORRHOIDAL PADS
witch hazel, lidocaine, phenylephrine hydrochloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55239-459 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 500 mg in 1 g LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 50 mg in 1 g PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55239-459-00 100 in 1 JAR 01/15/2024 1 2 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 01/15/2024 Labeler - Kleen Test Products Corporation (168165814)