PHARMBANNER Arnica Bruise Cream

Manufacturer
Shenzhen Xinxin Yunhai Technology Co., Ltd. | Jiangxi Zhongletang Pharmaceuticals Co., Ltd.
Effective date
2026-02-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:45:55

Label at a glance#

ProductPHARMBANNER Arnica Bruise Cream
Active ingredientCLOTRIMAZOLE
Label structure14 sections

Dosage and administration

■ 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.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 7%

Purpose

OTC - PURPOSE SECTION

Bruise, Pain & Swelling Relief

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

to broken skin or open wounds.

When Using

OTC - WHEN USING SECTION

avoid contact with eyes and mucous membranes.

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ 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

STORAGE AND HANDLING SECTION

■ 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

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Email us at: cs@pharmbanner.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CLOTRIMAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83818-023-01PHARMBANNER Arnica Bruise Cream113 g in 1 JARCREAM1132

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83818-02383818-023-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PHARMBANNER Arnica Bruise CreamARNICA BRUISE CREAMShenzhen Xinxin Yunhai Technology Co., Ltd.3c783061-8e2d-8a84-e063-6394a90a52652026-02-12WarningsExact identifier
ndc (package): 83818-023-01
ndc (product): 83818-023
ndc11 (package): 83818002301
spl id: 4aa15a3b-a40e-3a74-e063-6394a90a09cb
spl set id: 3c783061-8e2d-8a84-e063-6394a90a5265

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.