FDA.reportPublic FDA data

Active Ingredient

Manufacturer
Guangzhou Jingliang Cosmetics Co., Ltd.
Effective date
2026-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:38

Label at a glance#

ProductKOXUO Arnica Bruise Cream
Active ingredientARNICA MONTANA WHOLE
Label structure12 sections

Indications and uses

For the temporary relief of localized pain, itching, or discomfort from minor skin irritations.

Dosage and administration

Apply a small amount of Arnica cream to the affected area 2~3 times daily, Gently massage until fully absorbed.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

5% ARNICA

Ask a doctore before use

OTC - ASK DOCTOR SECTION

If pregnant or breast-feeding ask a health professional before use.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help.

Purpose

OTC - PURPOSE SECTION

pain relief

Stop Use

OTC - STOP USE SECTION

if irritation or rash develops

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Here are the ingredients extracted from the second image:

ARNICA MONTANA WHOLE

LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL

SYZYGIUM AROMATICUM WHOLE

MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)

BORNEOL

MAGNESIUM STEARATE

ETHYLHEXYL PALMITATE

CAPRYLIC/CAPRIC TRIGLYCERIDE

COPERNICIA CERIFERA (CARNAUBA) WAX

BEESWAX

MICROCRYSTALLINE WAX

STEARIC ACID

MENTHOL

BISABOLOL

BENTONITE

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount of Arnica cream to the affected area 2~3 times daily, Gently massage until fully absorbed.

Warnings

WARNINGS SECTION

For external use only.

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of localized pain, itching, or discomfort from minor skin irritations.

Do Not Use

OTC - DO NOT USE SECTION

Do not use on wounds or damaged skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Brand: KOXUO

Name: Arnica Bruise Cream

Size: 50 g

package designpackage design

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87408-016-01KOXUO Arnica Bruise Cream50 g in 1 BOTTLECREAM501
87408-016-01KOXUO Arnica Bruise Cream1 in 1 CARTONCREAM11

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87408-01687408-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVANDULA ANGUSTIFOLIA (LAVENDER) OILZBP1YXW0H8IACT
SYZYGIUM AROMATICUM WHOLEEY9MMA0P6YIACT
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE)461P5CJN6TIACT
BORNEOLM89NIB437XIACT
MAGNESIUM STEARATE70097M6I30IACT
ETHYLHEXYL PALMITATE2865993309IACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
COPERNICIA CERIFERA (CARNAUBA) WAXR12CBM0EIZIACT
BEESWAX2ZA36H0S2VIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
STEARIC ACID4ELV7Z65APIACT
ARNICA MONTANA WHOLEO80TY208ZWACTIB
MENTHOLL7T10EIP3AIACT
BISABOLOL24WE03BX2TIACT
BENTONITEA3N5ZCN45CIACT

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
KOXUO Arnica Bruise CreamARNICA BRUISE CREAMGuangzhou Jingliang Cosmetics Co., Ltd.5003bf83-fa01-b01a-e063-6294a90ad37f2026-04-21WarningsExact identifier
ndc (package): 87408-016-01
ndc (product): 87408-016
ndc11 (package): 87408001601
spl id: 5003ae61-788a-5a96-e063-6394a90a7d6b
spl set id: 5003bf83-fa01-b01a-e063-6294a90ad37f

Reported adverse events (FAERS/openFDA)#

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