CVS TOPICAL ANALGESIC HEMORRHOIDAL- dibucaine ointment

CVS Topical Analgesic Hemorrhoidal by

Drug Labeling and Warnings

CVS Topical Analgesic Hemorrhoidal by is a Otc medication manufactured, distributed, or labeled by CVS PHARMACY,INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Dibucaine 1%

Purpose

Local Anesthetic

Use

• temporarily relieves pain and itching due to hemorrhoids or other anorectal disorders

Warnings

For external use only.

Allergy alert  certain persons can develop allergic reactions to ingredients in this product. If the symptoms being treated do not subside or if redness, irritation, swelling, pain 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

• adults and children 12 years and over: if possible, clean the affected area with mild soap and warm water and rinse thoroughly. Dry by patting or blotting with toilet tissue or a soft cloth before applying.
• apply externally to the affected area up to 3 or 4 times daily.
• children under 12 years of age: ask a doctor.

Other information

• store at room temperature 68° - 77° F (20° - 25° C).
• tamper-evident: do not use if foil seal is broken or missing

Inactive ingredients

Lanolin, Light Mineral Oil, Purified Water, White Petrolatum

Package Labeling:

INGREDIENTS AND APPEARANCE

CVS TOPICAL ANALGESIC HEMORRHOIDAL 
dibucaine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-207
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIBUCAINE (UNII: L6JW2TJG99) (DIBUCAINE - UNII:L6JW2TJG99)	DIBUCAINE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
WATER (UNII: 059QF0KO0R)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-207-28	28 mL in 1 TUBE; Type 0: Not a Combination Product	02/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	02/14/2026

Labeler - CVS PHARMACY,INC (062312574)