Label: RAPIDOL HEMORRHOIDAL- glycerin, phenylephrine hcl, pramoxine hcl, white petrolatum cream
- NDC Code(s): 55758-448-01
- Packager: Pharmadel LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 30, 2024
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- Drug Facts
- Active ingredients & Purposes
- 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 of pharmacist before use if you are
presently taking a prescription drug for high blood pressure or depression
When using this product
- do not exceed the 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
- adults: when practical, cleanse the affected area with soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product
apply externally to the affected area after a bowel movement, no more than 4 times daily
- children under 12 years of age: consult a doctor
- Other information
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Inactive Ingredients
aloe vera leaf, alpha tocopherol (Vit. E), butylated hydroxyanisole, carboxymethylcellulose sodium, cetostearyl alcohol, cetyl alcohol, citric acid monohydrate, edetate disodium, glyceryl monostearate, methylparaben, mineral oil, panthenol, propylparaben, sodium benzoate, steareth-20, xanthan gum, water
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INGREDIENTS AND APPEARANCE
RAPIDOL HEMORRHOIDAL
glycerin, phenylephrine hcl, pramoxine hcl, white petrolatum creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55758-448 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 14.4 g in 100 g PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 0.25 g in 100 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 1 g in 100 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 15 g in 100 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) PANTHENOL (UNII: WV9CM0O67Z) XANTHAN GUM (UNII: TTV12P4NEE) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) SODIUM BENZOATE (UNII: OJ245FE5EU) STEARETH-20 (UNII: L0Q8IK9E08) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ALOE VERA LEAF (UNII: ZY81Z83H0X) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55758-448-01 1 in 1 CARTON 08/30/2024 1 30 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 08/30/2024 Labeler - Pharmadel LLC (030129680)