Label: GNP HEMORRHOIDAL MAXIMUM STRENGTH- hemorrhoidal cream
- NDC Code(s): 46122-776-37
- Packager: Amerisourcebergen Drug Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 25, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
-
Uses
-for temporary relief of pain, soreness, and burning.
-helps relieve the local itching and discomfort associated with hemorrhoids.
-temporarily shrinks hemorrhoidal tissue.
-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 a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children.
-
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 cream.
- when first opening the tube, puncture foil seal with top end of cap
- apply externally or in the lower portion of the anal canal only
- apply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
- for application in the lower anal canal: remove cover from dispensing cap. Attach dispensing cap to tube. Lubricate dispensing cap well, then gently insert dispensing cap partway into the anus.
- thoroughly cleanse dispensing cap after each use and replace cover
- children under 12 years of age: ask a doctor
- Other information
- Inactive ingredients
- Good Neighbor Pharmacy® Hemorrhoidal Pain Relief Cream 0.9 oz Carton Label
- Good Neighbor Pharmacy® Hemorrhoidal Pain Relief Cream 0.9 oz Tube Label
-
INGREDIENTS AND APPEARANCE
GNP HEMORRHOIDAL MAXIMUM STRENGTH
hemorrhoidal creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46122-776 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 150 mg in 1 g GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 144 mg in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 25 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MINERAL OIL (UNII: T5L8T28FGP) CETYL PALMITATE (UNII: 5ZA2S6B08X) ALOE (UNII: V5VD430YW9) SODIUM CITRATE (UNII: 1Q73Q2JULR) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) STEARIC ACID (UNII: 4ELV7Z65AP) LANOLIN (UNII: 7EV65EAW6H) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46122-776-37 1 in 1 CARTON 10/09/2024 1 25.5 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 10/09/2024 Labeler - Amerisourcebergen Drug Corporation (007914906) Registrant - Unipack LLC (009248480) Establishment Name Address ID/FEI Business Operations Unipack LLC 009248480 manufacture(46122-776)
