Label: HEMORRHOIDAL PAIN RELIEF- hemorrhoidal pain relief ointment ointment
- NDC Code(s): 13709-334-01
- Packager: Neilmed Pharmaceuticals Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 11, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Drug Facts:
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Uses:
- Helps relieve the local itching and discomfort associated with hemorrhoids
- Temporarily shrinks hemorrhoidal 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
- Warnings:
- Ask a doctor before use if you have:
- Ask a doctor or pharmacist before use if you are:
- When using this product:
- Stop use and ask doctor if:
- If pregnant or breast-feeding:
- Keep out of reach of children.
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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.
- When first opening the tube, puncture foil seal with top end of cap.
- 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 the 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.
- Other Information:
- Inactive ingredients:
- Questions or comments?
- Important:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HEMORRHOIDAL PAIN RELIEF
hemorrhoidal pain relief ointment ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:13709-334 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 749 mg in 1 g MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL 140 mg in 1 g PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 2.5 mg in 1 g Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) PARAFFIN (UNII: I9O0E3H2ZE) WATER (UNII: 059QF0KO0R) THYMUS VULGARIS (THYME) OIL (UNII: 2UK410MY6B) LANOLIN (UNII: 7EV65EAW6H) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERIN (UNII: PDC6A3C0OX) BENZOIC ACID (UNII: 8SKN0B0MIM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) LANOLIN ALCOHOL (UNII: 884C3FA9HE) WHITE WAX (UNII: 7G1J5DA97F) CORN OIL (UNII: 8470G57WFM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13709-334-01 1 in 1 CARTON 06/11/2025 1 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 06/11/2025 Labeler - Neilmed Pharmaceuticals Inc. (799295915) Establishment Name Address ID/FEI Business Operations Neilmed Pharmaceuticals Inc. 799295915 manufacture(13709-334)

