Label: RRHOID RAGE HEMORRHOIDAL- lidocaine, phenylephrine hydrochloride ointment
- NDC Code(s): 82433-446-00
- Packager: POPPY COLLECTIVE LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 31, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
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Uses
–Helps relieve the pain, itching, and burning associated with hemorrhoids.
–Temporarily reduces the swelling associated with irritated hemorrhoidal tissue and other anorectal disorders.
–Temporarily provides a coating for relief of anorectal discomforts.
–Temporarily protects irritated areas and inflamed perianal skin.
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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 or pharmacist before use if you are
presently taking a prescription drug for high blood pressure or depression.
When using this product
–Avoid contact with eyes.
–Do not exceed recommended daily dosage unless directed by a doctor.
–Do not put this product into the rectum by using fingers or any mechanical device or applicator.
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Directions
–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 soft cloth before applying.
–Adults and children 12 years and older: apply externally to the affected area up to 4 times daily.
–Children under 12 years of age: consult a doctor.
- Other information
- Inactive ingredients
- Package Labeling:
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INGREDIENTS AND APPEARANCE
RRHOID RAGE HEMORRHOIDAL
lidocaine, phenylephrine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82433-446 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 HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) GLYCERIN (UNII: PDC6A3C0OX) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) PROPYLPARABEN (UNII: Z8IX2SC1OH) WITCH HAZEL (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82433-446-00 1 in 1 BOX 02/12/2024 1 28 g in 1 TUBE; 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 02/12/2024 Labeler - POPPY COLLECTIVE LLC (035330878)