Camphor - Aidance Skincare & Topical Solutions, LLC

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2019-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:02:41

Label at a glance#

ProductCBD Clinic Deep-Rub Pain Relief - Level 1
Active ingredientCAMPHOR (NATURAL)
Label structure8 sections

Indications and uses

temporarily relieves minor aches and pain of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Dosage and administration

• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily Wash hands with soap and water after use (unless applying to hands) • children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor USP, 3%

Purpose

OTC - PURPOSE SECTION

Camphor - Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pain of muscles and joints associated with:
• simple backache • arthritis • strains • bruises • sprains

Warnings

WARNINGS SECTION

For external use only
Do not use on
• wounds or damaged skin
When using this product
• avoid contact with eyes or mucous membranes
• do not bandage tightly or use with a heating pad
Stop use and ask a doctor if
• condition worsens
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation develops
If pregnant or breast-feeding
ask a health professional before use
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center immediately 

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• adults and children 12 years of age and older:
apply to affected area not more than 3 to 4 times daily
Wash hands with soap and water after use (unless applying to hands)
• children under 12 years of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CBD hemp oil, clove oil, cottonseed oil, eucalyptus oil, jojoba seed oil, tea tree oil

Questions?

SPL UNCLASSIFIED SECTION

Call 1-888-422-3254

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24909-752-12CBD Clinic Deep-Rub Pain Relief - Level 1355 mL in 1 BOTTLEOIL3551
24909-752-28CBD Clinic Deep-Rub Pain Relief - Level 13785 mL in 1 BOTTLEOIL37851
24909-752-64CBD Clinic Deep-Rub Pain Relief - Level 11893 mL in 1 BOTTLEOIL18931

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24909-752CBD CLINIC DEEP-RUB PAIN RELIEF - LEVEL 1 (CAMPHOR) OIL [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]1Legacy NDC, 3 package rows20200101_bcf4a471-ae5f-4579-8eb9-aa8ec00aa4d8.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-75224909-752-12, 24909-752-28, 24909-752-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
e2b71735-d669-4cef-88bc-f03f6fa315d5bcf4a471-ae5f-4579-8eb9-aa8ec00aa4d82019-12-29WarningsExact identifier
spl id: e2b71735-d669-4cef-88bc-f03f6fa315d5
spl set id: bcf4a471-ae5f-4579-8eb9-aa8ec00aa4d8

Reported adverse events (FAERS/openFDA)#

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