DR.SEYMOUR BUTTS HEMORRHOID- lidocaine 5% phenylephrine hcl 0.25% hemorrhoid ointment

Dr.Seymour Butts Hemorrhoid by

Drug Labeling and Warnings

Dr.Seymour Butts Hemorrhoid by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine 5% Phenylephrine HCl 0.25%

Purpose

Local anesthetic，Vasoconstrictor

Use

Temporarily shrinks hemorrhoidal tissue and relieves pain, soreness,
burning, itching, and discomfort associated with hemorrhoids.

Warnings

For external use only Allergy alert: do not use if you have a history of allergy to amide-type
local anesthetics (e.g., lidocaine).

Do not use

if the tube seal is broken or missing in children under 12 years of age
unless directed by a doctor for more than 7 days unless directed by a
doctor

When Using

avoid contact with eyes do not exceed the recommended dosage
unless directed by a doctor do not put this product into the rectum (use
the applicator as directed) if introduction of applicator causes additional
pain, stop use and ask a docto

Stop Use

bleeding occurs condition worsens or does not improve within 7 days
redness, irritation, swelling, pain, or rash develops
If pregnant or breast-feeding, ask a health professional before use.

Ask Doctor

heart disease, high blood pressure, thyroid disease, or diabetes
difficulty urinating due to an enlarged prostate allergies to amide-type
local anesthetics

Keep Oot Of Reach Of Children

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

Directions

Adults: When practical, cleanse the affected area with mild soap and
warm water, rinse thoroughly, and gently dry. Apply to the affected area
up to 4 times daily, especially at night, in the morning, and after each
bowel movement. To use applicator: lubricate applicator; gently insert
partway into the anal canal and apply a small amount. Clean applicator
after each use.
Children under 12 years of age: ask a doctor.

Other information

Store at 20–25°C (68–77°F).

Inactive ingredients

Purified Water，Witch Hazel Extract, Aloe Vera Extract, Boswellia serrata Extract, Sophora，
japonica Extract, Calendula Extract, Centella asiatica Extract, Vitamin E
(Tocopherol), Tocopheryl Acetate, Petrolatum USP, Shea Butter, Glycerin,
Caprylic/Capric Triglycerides (MCT), Cetearyl Alcohol, Glyceryl Stearate,
PEG-100 Stearate, Phenoxyethanol, Ethylhexylglycerin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.SEYMOUR BUTTS HEMORRHOID 
lidocaine 5% phenylephrine hcl 0.25% hemorrhoid ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-189
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	0.25 g  in 100 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PETROLATUM (UNII: 4T6H12BN9U)
GLYCERIN (UNII: PDC6A3C0OX)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WITCH HAZEL (UNII: 101I4J0U34)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
SWERTIA JAPONICA WHOLE FLOWERING (UNII: 01X0P6GX6C)
BOSWELLIA SERRATA GUM (UNII: 4PW41QCO2M)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
SHEA BUTTER (UNII: K49155WL9Y)
WATER (UNII: 059QF0KO0R)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CALENDULA ARVENSIS LEAF (UNII: 3U3U118F2L)
BAPTISIA ALBA WHOLE (UNII: 104HF4767P)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-189-01	30 g in 1 TUBE; Type 0: Not a Combination Product	09/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	09/26/2025

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-189)