Label: RAPIDOL- hydrocortisone cream
- NDC Code(s): 55758-420-02
- Packager: Pharmadel LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 29, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient & Purpose
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Uses
For the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to
- eczema
- insect bites
- poison ivy
- poison oak
- poison sumac
- soaps
- detergent
- cosmetics
- jewelry
- seborrheic dermatitis
- psoriasis
- and for external feminine, genital, and anal itching
- for other uses of this product should only be under the advice and supervision of a doctor
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Warnings
FOR EXTERNAL USE ONLY. Avoid contact with the eyes.
Do not use
- for treatment of diaper rash. Consult a doctor
- if you have a vaginal discharge. Consult a doctor.
- with any other hydrocortisone product unless you have consulted a doctor
When using this product
- for external anal itching: Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator.
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Directions
For itchy skin, irritations, inflammation, rashes and external feminine and genital itching:
- adults and children 2 years of age and older: apply to the affected area not more than 3 to 4 times daily.
- children under 2 years of age: do not use, consult a doctor
For external anal itching:
- adults: 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 a soft cloth before application of this product.
- children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
RAPIDOL
hydrocortisone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55758-420 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHYL SULFOXIDE (UNII: YOW8V9698H) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) Product Characteristics Color white (Off white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55758-420-02 1 in 1 CARTON 06/30/2024 1 60 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 M017 06/30/2024 Labeler - Pharmadel LLC (030129680)
