NUPERCAINAL- dibucaine ointment 
Dr. Reddy's Laboratories Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Nupercainal®

Drug Facts

Active ingredient

Dibucaine 1%

Purpose

Hemorrhoidal ointment

Use

Warnings

For external use only

Allergy alert

  • certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, 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 within 7 days

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

Inactive ingredients

acetone sodium bisulfite, lanolin, light mineral oil, purified water, white petrolatum

Questions?

call 1-800-790-6417

PRINCIPAL DISPLAY PANEL - 56.7g Tube Box

LONGEST LASTING
INGREDIENT

UP TO 8 HOURS

NDC 55741-402-02

NUPERCAINAL®
HEMORRHOIDAL OINTMENT

DIBUCAINE 1%

Fast Temporary Relief of Pain, Itching,
and Burning Due to Hemorrhoids.

NET WT 2 oz. (56.7g)

Principal Display Panel - 56.7g Tube Box
NUPERCAINAL 
dibucaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55741-402
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dibucaine (UNII: L6JW2TJG99) (Dibucaine - UNII:L6JW2TJG99) Dibucaine1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
acetone sodium bisulfite (UNII: 47VY054OXY)  
lanolin (UNII: 7EV65EAW6H)  
light mineral oil (UNII: N6K5787QVP)  
water (UNII: 059QF0KO0R)  
petrolatum (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55741-402-021 in 1 BOX05/24/2016
156.7 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34605/24/2016
Labeler - Dr. Reddy's Laboratories Inc. (802315887)

Revised: 6/2016
Document Id: c7a5c1fa-7822-8e8b-09e6-18156ad6c7bc
Set id: bcf33951-d3a4-46c5-b208-56adc0011047
Version: 3
Effective Time: 20160615
 
Dr. Reddy's Laboratories Inc.