PHARMBANNER ARNICA BRUISE CREAM- arnica bruise cream cream

PHARMBANNER Arnica Bruise Cream by

Drug Labeling and Warnings

PHARMBANNER Arnica Bruise Cream by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xinxin Yunhai Technology Co., Ltd., Jiangxi Zhongletang Pharmaceuticals Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Arnica Montana 7%

Purpose

Bruise, Pain & Swelling Relief

Use

Temporarily relieves: Bruising, Swelling, Minor muscle or joint pain.
Helps reduce skin discoloration and tenderness from
everyday bumps, overuse, or minor injuries.

Warnings

For external use only.

Do not use

to broken skin or open wounds.

When Using

avoid contact with eyes and mucous membranes.

Stop Use

Rash or irritation occurs;
Symptoms persist for more than 7 days or worsen.

Ask Doctor

Rash or irritation occurs;
Symptoms persist for more than 7 days or worsen.

Keep Out Of Reach Of Children

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

Directions

■ Apply a thin layer to affected area 2–3 times daily.
■ Gently massage until fully absorbed.
■ Use consistently for best results.
■ Wash hands after use.

Other information

■ Store at 20–25°C (68–77°F)
■ Do not use if safety seal is broken
■ Keep away from direct sunlight and excessive heat

Inactive ingredients

Water (Aqua), Shea Butter, Coconut Oil (Cocos NuciferaOil), Centella Asiatica Extract, Tocopheryl Acetate
(Vitamin E), Ascorbyl Palmitate (Vitamin C), Glycerin, Carbomer, Phenoxyethanol, Ethylhexylglycerin, Sodium Hydroxide

Questions

Email us at: cs@pharmbanner.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PHARMBANNER ARNICA BRUISE CREAM 
arnica bruise cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83818-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOTRIMAZOLE (UNII: G07GZ97H65) (CLOTRIMAZOLE - UNII:G07GZ97H65)	CLOTRIMAZOLE	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SHEA BUTTER (UNII: K49155WL9Y)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
CARBOMER (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83818-023-01	113 g in 1 JAR; Type 0: Not a Combination Product	08/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/16/2025

Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co., Ltd.		411295811	manufacture(83818-023)