FDA.reportPublic FDA data

Skinade MD INsupport

Manufacturer
Bottled Science, Inc.
Effective date
2025-10-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:35:15

Label at a glance#

ProductSkinade MD INsupport
Active ingredientARNICA MONTANA, LEDUM PALUSTRE WHOLE, CALENDULA OFFICINALIS FLOWER, HYPERICUM PERFORATUM FLOWER, BELLIS PERENNIS, SULFURIC ACID, ALLYLTHIOUREA, PHYLLOQUINONE OMEGA-HYDROXYLASE CYP4F11
Label structure10 sections

Indications and uses

Reduces bruising and swelling, improves healing, promotes wound healing

Dosage and administration

Take 3 sprays 4-5 times per day or as directed. See pack or insert for full information

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Contains 0.25% of each of the following HPUS ingredients:

Active IngredientsPurpose
Arnica Montana 30C, 200CkReduces bruising and swelling
Ledum Palustre 30CImproves healing
Calendula Officinalis 30CPromotes wound healing
Bellis Perennis 30CReduces soft tissue swelling
Hypericum Perforatum 30CReduces pain
Sulphuricum Acidum 30CReduces bruising
Thiosinaminum 30CReduces scarring
Phylloquinone (Vit.K1) 3CTargets bruising

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If pregnant or breast feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Take 3 sprays 4-5 times per day or as directed. See pack or insert for full information

Other Information

OTHER SAFETY INFORMATION

Do not use if cap seal is broken or missing. Store at room temperature, away from direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl Alcohol 20%, purified water, vegetable glycerin 10%

Indications and Usage

INDICATIONS & USAGE SECTION

Reduces bruising and swelling, improves healing, promotes wound healing

Purpose

OTC - PURPOSE SECTION

Reduces bruising and swelling

Improves healing

Promotes wound healing

Reduces soft tissue swelling

Reduces pain

Reduces bruising

Reduces scarring

Targets bruising

Warnings

WARNINGS SECTION

Claims based on traditional Homeopathic practive, not accepted medical evidence. Not FDA evaluated

RECENT MAJOR CHANGES SECTION

Dosage updated to recommend consulting Pack or Insert for full information

Indications and Usage section updated

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Skinade MD Post CareSkinade MD Post CareSkinade_MD_packaging_Spray bottle label_US_11.11.2025 copy.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73130-004-25Skinade MD INsupport25 mL in 1 BOTTLE, SPRAYSPRAY254

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73130-00473130-004-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
ARNICA MONTANAO80TY208ZWACTIB
LEDUM PALUSTRE WHOLE1N8KG72C5MACTIB
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDACTIB
HYPERICUM PERFORATUM FLOWERA6V4CUE7PVACTIB
BELLIS PERENNIS2HU33I03UYACTIB
SULFURIC ACIDO40UQP6WCFACTIB
ALLYLTHIOUREA706IDJ14B7ACTIB
PHYLLOQUINONE OMEGA-HYDROXYLASE CYP4F11NKU2TZDAK2ACTIB

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
Skinade MD INsupportARNICA, LEDUM, CALENDULA, BELLIS PERENNIS, HYPERICUM PERF. SULPH.AC., THIOSINAMINUM, VIT.K1Bottled Science, Inc.eb0069b3-8f68-3f41-e053-2995a90adbac2025-10-16WarningsExact identifier
ndc (package): 73130-004-25
ndc (product): 73130-004
ndc11 (package): 73130000425
spl id: 414c0271-6adb-10bf-e063-6394a90ab7d8
spl set id: eb0069b3-8f68-3f41-e053-2995a90adbac

Reported adverse events (FAERS/openFDA)#

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