Label: HEMORRHOIDAL- mineral, petrolatum, phenylephrine hydrochloride ointment
- NDC Code(s): 51316-228-01, 51316-228-02
- Packager: CVS PHARMACY, INC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 25, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
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Uses
- helps relieve the local itching and discomfort associated with hemorrhoids
- temporarily shrinks hemorrhoid tissue and relieves burning
- temporarily provides a coating for relief of anorectal discomforts
- temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful
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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.
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Directions
Adults:
- when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying ointment.
- apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
- intrarectal use: remove cover from applicator, attach applicator to tube, lubricate applicator well and gently insert applicator into the rectum, thoroughly cleanse applicator after each use and replace cover
- also apply ointment to external area
- regular use provides continual therapy for relief of symptoms
- Children under 12 years of age: ask a doctor.
- Other information
- Inactive ingredients
- Questions?
- Package Labeling: HEMORRHOIDAL OINTMENT, 1oz/28g
- Package Labeling: HEMORRHOIDAL OINTMENT, 2oz/57g
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INGREDIENTS AND APPEARANCE
HEMORRHOIDAL
mineral, petrolatum, phenylephrine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-228 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 140 mg in 1 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 749 mg in 1 g PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) BENZOIC ACID (UNII: 8SKN0B0MIM) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-228-01 1 in 1 BOX 06/15/2022 1 28 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:51316-228-02 1 in 1 BOX 06/15/2022 2 57 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 06/15/2022 Labeler - CVS PHARMACY, INC (062312574)