DIBUCAINE TOPICAL ANESTHETIC 1% HEMORRHOIDAL- dibucaine ointment 
Rugby Laboratories Inc.

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Dibucaine Topical Anesthetic 1% Hemorrhoidal Ointment

​Drug Facts

​Active ingredient

Dibucaine 1%

​Purpose

Hemmorhoidal ointment

​Use

​Warnings

​For external use only.

Allergy Alert

  • Certain persons can develop allergic reactions to ingredients in this product.  If the symptoms being treated does not subside or if redness, irritaion, swelling, bleeding or other symptoms develop or increase, discontinue use and ask a doctor.

Do not use

  • in or near the eyes
  • in children under 2 years of age

When using this product

  • do not use more than directed unless directed by a doctor.
  • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

  • bleeding occurs
  • condition worsens or does not improve

If pregnant or breast-feeding

ask a health care 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

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Lanolin, Light Mineral Oil, Purified Water, White Petrolatum

Questions or comments?

call 1-800-645-2158

Package Labeling:

Package 1 OZ

DIBUCAINE TOPICAL ANESTHETIC 1% HEMORRHOIDAL 
dibucaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0536-1211
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIBUCAINE (UNII: L6JW2TJG99) (DIBUCAINE - UNII:L6JW2TJG99) DIBUCAINE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN (UNII: 7EV65EAW6H)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0536-1211-951 in 1 BOX08/19/2019
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01508/19/2019
Labeler - Rugby Laboratories Inc. (079246066)

Revised: 10/2023
Document Id: 08833e99-3ddc-97e6-e063-6294a90abc6e
Set id: f23c8cd1-98f9-41cd-84d4-cf01c2ede29a
Version: 5
Effective Time: 20231024
 
Rugby Laboratories Inc.