FDA.reportPublic FDA data

EARTHS CARE MUSCLE AND JOINT RUB

Manufacturer
DLC Laboratories, Inc.
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:31:46

Label at a glance#

ProductEARTHS CARE MUSCLE AND JOINT RUB
Active ingredientCAMPHOR (NATURAL)
Label structure10 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: bruises simple backache arthritis strains sprains

Dosage and administration

adults and children 2 years of age or older: apply to affected area not more than 3 or 4 times daily avoid overuse on large areas of the skin children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 3%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

  • bruises
  • simple backache
  • arthritis
  • strains
  • sprains

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • with a heating pad
  • on wounds or damaged skin

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes and mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • skin redness or excessive irritation of the skin develops
  • symptoms clear up and occur again within a few days
  • condition worsens or if symptoms persist for more than 7 days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age or older:apply to affected area not more than 3 or 4 times daily
  • avoid overuse on large areas of the skin
  • children under 2 years of age:consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Arnica montana(arnica) flower extract, beeswax, Butyrospermum parkii(shea) butter, Eucalyptus globulus(eucalyptus) oil, Gaultheria procumbensL .(wintergreen) oil, Heterotheca inuloidesflower extract, Matricaria recutita(chamomile) flower extract, Melaleuca cajeputi(cajeput) oil, Myroxylon pereirae(balsam peru), Prunus amygdalus dulcis(sweet almond) oil, Rosmarinus officinalis(rosemary) extract, tocopherol (natural vitamin E)

Questions?

OTC - QUESTIONS SECTION

call 1-888-602-6380

SPL UNCLASSIFIED SECTION

Distributed by:
Earth's Care Natural Products, Inc.
Long Beach, California 90805 USA

PRINCIPAL DISPLAY PANEL - 71 g Jar Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EARTH'S
CARE ™

Allergy
Tested

PARABEN
FREE

Muscle & Joint Rub

Bruises, Aches and Strains

Camphor / External Analgesic

with Arnica montana

2.5 OZ. (71 g)

1%
FOR THE
PLANET ℠
MEMBER

Principal Display Panel - 71 g Jar Box
Principal Display Panel - 71 g Jar Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249111camphor 3 % Topical OintmentPSN5
1249111camphor 0.03 MG/MG Topical OintmentSCD5
1249111camphor 3 % Topical OintmentSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24286-1563-2EARTHS CARE MUSCLE AND JOINT RUB71 g in 1 JAROINTMENT715
24286-1563-2EARTHS CARE MUSCLE AND JOINT RUB1 in 1 BOXOINTMENT15
24286-1563-3EARTHS CARE MUSCLE AND JOINT RUB2.8 g in 1 POUCHOINTMENT2.85

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9411
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9411
ALMOND OILINACTIVE INGREDIENT66YXD4DKO91
ARNICA MONTANA FLOWERINACTIVE INGREDIENTOZ0E5Y15PZ1
BALSAM PERUINACTIVE INGREDIENT8P5F881OCY1
CAJUPUT OILINACTIVE INGREDIENTJ3TO6BUQ371
CHAMOMILEINACTIVE INGREDIENTFGL3685T2X1
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI6621
HETEROTHECA INULOIDES FLOWERINACTIVE INGREDIENTW9NZ9OZF681
METHYL SALICYLATEINACTIVE INGREDIENTLAV5U5022Y1
ROSEMARYINACTIVE INGREDIENTIJ67X351P91
SHEA BUTTERINACTIVE INGREDIENTK49155WL9Y1
TOCOPHEROLINACTIVE INGREDIENTR0ZB2556P81

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
24286-156324286-1563-2, 24286-1563-3

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
BALSAM PERU8P5F881OCYIACT
CAJUPUT OILJ3TO6BUQ37IACT
CHAMOMILEFGL3685T2XIACT
EUCALYPTUS OIL2R04ONI662IACT
ROSEMARYIJ67X351P9IACT
SHEA BUTTERK49155WL9YIACT
ALMOND OIL66YXD4DKO9IACT
TOCOPHEROLR0ZB2556P8IACT
METHYL SALICYLATELAV5U5022YIACT
HETEROTHECA INULOIDES FLOWERW9NZ9OZF68IACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 18 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YPOWDER / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YGEL / TOPICAL0.05 %w/wExact identifier — unii+route
6 equally ranked IID candidates
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YGEL / TOPICAL0.05 %w/wExact identifier — unii+route
6 equally ranked IID candidates
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YPOWDER / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
TOCOPHEROLTOCOPHEROLR0ZB2556P8CREAM / TOPICALNAExact identifier — unii+route
3 equally ranked IID candidates
ALMOND OILALMOND OIL66YXD4DKO9CREAM / TOPICAL2 %w/wExact identifier — unii+route
3 equally ranked IID candidates
TOCOPHEROLTOCOPHEROLR0ZB2556P8CREAM / TOPICALNAExact identifier — unii+route
3 equally ranked IID candidates
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate
3 equally ranked IID candidates
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate
3 equally ranked IID candidates
ALMOND OILALMOND OIL66YXD4DKO9CREAM / TOPICAL2 %w/wExact identifier — unii+route
3 equally ranked IID candidates
SHEA BUTTERSHEA BUTTERK49155WL9YLOTION / TOPICAL2340 mgExact identifier — unii+route
3 equally ranked IID candidates
SHEA BUTTERSHEA BUTTERK49155WL9YLOTION / TOPICAL2340 mgExact identifier — unii+route
3 equally ranked IID candidates
SHEA BUTTERSHEA BUTTERK49155WL9YLOTION / TOPICAL2340 mgExact identifier — unii+route
3 equally ranked IID candidates
ALMOND OILALMOND OIL66YXD4DKO9CREAM / TOPICAL2 %w/wExact identifier — unii+route
3 equally ranked IID candidates
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YGEL / TOPICAL0.05 %w/wExact identifier — unii+route
6 equally ranked IID candidates
METHYL SALICYLATEMETHYL SALICYLATELAV5U5022YPOWDER / TOPICALNAExact identifier — unii+route
6 equally ranked IID candidates
TOCOPHEROLTOCOPHEROLR0ZB2556P8CREAM / TOPICALNAExact identifier — unii+route
3 equally ranked IID candidates
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate
3 equally ranked IID candidates

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
EARTHS CARE MUSCLE AND JOINT RUBCAMPHORDLC Laboratories, Inc.71e33e06-4dc3-4ead-a122-ff89d93a64de2026-01-07WarningsExact identifier
ndc (package): 24286-1563-2
ndc (package): 24286-1563-3
ndc (product): 24286-1563
ndc11 (package): 24286156302
ndc11 (package): 24286156303
spl id: 47d51ea3-402f-7c95-e063-6394a90a3e8e
spl set id: 71e33e06-4dc3-4ead-a122-ff89d93a64de

Reported adverse events (FAERS/openFDA)#

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