Skinuva Bruise

Manufacturer
MD Medical Designs, Inc.
Effective date
2026-02-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:36:59

Label at a glance#

ProductSkinuva Bruise
Active ingredientARNICA MONTANA
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                                  Purpose*

Arnica montana 30X HPUS..............Bruising, swelling, pain and

                                                                  anti-inflammatory

HPUS indicates that the ingredient is officially included in the

Homeopathic Pharmacopoeia of the United States

*Claims based on traditional homeopathic practice, not accepted

medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION

UsesReduces pain, swelling, and discoloration from bruises.

Temporarily relieves muscle pain and stiffness due to surgery and injury.

WARNINGS SECTION

Warnings

Use only as directed. Consult your physician on the use of this product.

Keep out of reach of children.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

Take 2 capsules per day or as directed by your physician.

OTHER SAFETY INFORMATION

Other informationDo not use if inner seal is broken.

Store in a cool, dark and dry place. If symptoms worsen or persist

for more than 7 days, consult your physician.

INACTIVE INGREDIENT SECTION

Inactive ingredientsascorbic acid, bromelain,

cellulose (capsule shell), grape seed extract, magnesium stearate,

maltodextrin, rutin, sucrose, zinc oxide

OTC - QUESTIONS SECTION

Dist. by: MD Medical Designs, Inc.,

Beverly Hills, CA 90212 ● Manufactured in U.S.A.

FDA Registered

www.skinuva.com

SOTC14Rev03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SKINUVA

bruise

Arnica + Bromelain + Zinc

with other antioxidatants

*Reduces bruising, swelling, and pain

from surgeries, cosmetic procedures,

and injuries

14 Vegetarian Capsules

Homeopathic Medicine

Vegan | Gluten Free | Non-GMO

SKINUVA BRUISE LABELSKINUVA BRUISE LABEL

OTC - PURPOSE SECTION

UsesReduces pain, swelling, and discoloration from bruises.

Temporarily relieves muscle pain and stiffness due to surgery and injury

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130723042304522GTIN-13: 0723042304522
EAN-13: 0723042304522
GTIN-12: 723042304522
UPC-A: 723042304522
GTIN storage (14 digits): 00723042304522
skn.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82350-001-14Skinuva Bruise14 in 1 BOTTLE, PLASTICCAPSULE142

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82350-00182350-001-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Skinuva BruiseARNICA MONTANA, BROMELAIN, GRAPE SEED EXTRACT, VITAMIN C, RUTIN, ZINC OXIDE, CELLULOSEMD Medical Designs, Inc.8bf57652-5750-4111-acef-45c5fdc676af2026-02-09WarningsExact identifier
ndc (package): 82350-001-14
ndc (product): 82350-001
ndc11 (package): 82350000114
spl id: 4a7126f7-bc85-b6d9-e063-6394a90a23bc
spl set id: 8bf57652-5750-4111-acef-45c5fdc676af

Reported adverse events (FAERS/openFDA)#

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