DRS PHARMACY HEMORRHOIDAL- phenylephrine hcl ointment 
OL PHARMA TECH, LLC Drs PHARMACY

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ACTIVE INGREDIENTS

  1. Phenylephrine HCI, 0.25%
  2. Petrolatum 74.9 %
  3. mineral oil 14 %

PURPOSE

USES

WARNINGS

For external use only and / or intrarectal use only

ASK A DOCTOR BEFORE USE IF YOU HAVE

Ask a doctor or pharmacist before use if you are

presently taking a prescription drug for high blood pressure or depression

WHEN USING THIS PRODUCT

STOP USING AND ASK YOUR DOCTOR IF

IF PREGNENT OR BREAST-FEEDING

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

OTHER INFORMATION

store at 20-25°C (68-77°F)

INACTIVE INGREDIENTS

methylparaben, propylparaben, purified water, benzoic acid, butylated hydroxyanisole, corn oil, glycerine, lanolin, lanolin alcohols, mineral oil, paraffin, tocopherol, white wax

QUESTIONS

www.drspharmacyusa.com

hemorrhoidal ointment

DRS PHARMACY HEMORRHOIDAL 
phenylephrine hcl ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-956
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM749 mg  in 1 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 mg  in 1 g
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL140 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZOIC ACID (UNII: 8SKN0B0MIM)  
PARAFFIN (UNII: I9O0E3H2ZE)  
CORN OIL (UNII: 8470G57WFM)  
GLYCERIN (UNII: PDC6A3C0OX)  
THYME (UNII: CW657OBU4N)  
WHITE WAX (UNII: 7G1J5DA97F)  
TOCOPHEROL (UNII: R0ZB2556P8)  
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
WATER (UNII: 059QF0KO0R)  
LANOLIN (UNII: 7EV65EAW6H)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80489-956-011 in 1 CARTON11/01/2021
128.3 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01511/01/2021
Labeler - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
Establishment
NameAddressID/FEIBusiness Operations
OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-956)

Revised: 4/2024
Document Id: 16426f2d-8934-2e33-e063-6294a90aac05
Set id: 164169b9-0627-9d1a-e063-6294a90ac46d
Version: 2
Effective Time: 20240416
 
OL PHARMA TECH, LLC Drs PHARMACY