FDA.reportPublic FDA data

Earth's Care Pain Relieving Ointment

Manufacturer
DLC Laboratories, Inc.
Effective date
2026-07-28
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
daily-update
Hydrated at
2026-07-31 05:10:25

Label at a glance#

ProductEarths Care Pain Relieving
Active ingredientCAMPHOR (NATURAL), MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE
Label structure8 sections

Indications and uses

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

Dosage and administration

use only as directed adults and children 12 years of age and older:  apply to affected area not more than 3 or 4 times daily. avoid overuse on large areas of the skin wash hands thoroughly after application children under 12 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 4%

Menthol 10%

Methyl Salicylate (Wintergreen Oil) 15%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only.

Allergy Alert:If you are allergic to aspirin or salicylates, consult a doctor before use.

Do not use

OTC - DO NOT USE SECTION

  • with a heating pad or other heat sources (may blister skin)
  • on children under 12 years of age
  • on wounds or damaged skin
  • if you are taking anticoagulant medication

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if here is redness over the affected area.

When using this product

OTC - WHEN USING SECTION

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

Stop 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

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 right away.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • use only as directed
  • adults and children 12 years of age and older:  apply to affected area not more than 3 or 4 times daily.
  • avoid overuse on large areas of the skin
  • wash hands thoroughly after application
  • children under 12 years of age: consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

beeswax, Butyrospermum parkii (shea) butter, Prunus amygdalus dulcis (sweet almond) oil, Rosmarinus officinialis (rosemary) extract, tocopherol (natural vitamin E)

Questions?

OTC - QUESTIONS SECTION

call 1-888-602-6380

SPL UNCLASSIFIED SECTION

Origins

Natural Camphor is found in the wood of the Camphor Laurel tree (Cinnamomum camphora), an evergreen species from Asia. Natural Menthol is a substance found in peppermint and in other mint oils. Natural Wintergreen Oil is extracted from the leaves of wintergreen plants such as the Eastern Teaberry (Gaultheria procumbens).

Indications

Earth's Care Pain Relieving Ointment is a powerful blend of three natural ingredients that provide soothing, penetrating relief from sore muscles, joint pain, backache and minor arthritis. Our proprietary formula features naturally-sourced Camphor, Menthol and Wintergreen Oil that together work as an effective analgesic without parabens or phthalates.

  • No Preservatives
  • No Animal Testing
  • No Artificial Colors or Fragrances
  • No Petrolatum

Triple Action Formula:

  • Camphor
  • Menthol
  • Wintergreen Oil

RETAIN CARTON FOR COMPLETE DRUG FACTS.

Distributed by:
Earth's Care Natural Products, Inc.
Long Beach, California 90805 USA
Questions: 1-888-602-6380

earths-care.com

PRINCIPAL DISPLAY PANEL - 71 g Jar Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EARTH'S
CARE ®

Allergy
Tested

PARABEN
FREE

TRIPLE ACTION

Pain Relieving
Ointment

Relieves Minor Backache,
Sprains, Muscle & Joint Pain

1%
FOR THE
PLANET
MEMBER

NET WT 2.5 OZ. (71 g)

labellabel

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9414
MENTHOLACTIVE INGREDIENTL7T10EIP3A4
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y4
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9414
MENTHOLACTIVE MOIETYL7T10EIP3A4
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ4
ALMOND OILINACTIVE INGREDIENT66YXD4DKO94
ROSEMARYINACTIVE INGREDIENTIJ67X351P94
SHEA BUTTERINACTIVE INGREDIENTK49155WL9Y4
TOCOPHEROLINACTIVE INGREDIENTR0ZB2556P84
YELLOW WAXINACTIVE INGREDIENT2ZA36H0S2V4

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24286-155424286-1554-2, 24286-1554-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
METHYL SALICYLATELAV5U5022YACTIB
YELLOW WAX2ZA36H0S2VIACT
ROSEMARYIJ67X351P9IACT
SHEA BUTTERK49155WL9YIACT
ALMOND OIL66YXD4DKO9IACT
TOCOPHEROLR0ZB2556P8IACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92025-05-15full-release2026-06-01 01:01:10

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 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALMOND OILALMOND OIL66YXD4DKO9CREAM / TOPICAL2 %w/wExact identifier — unii+route
3 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
ALMOND OILALMOND OIL66YXD4DKO9CREAM / TOPICAL2 %w/wExact identifier — unii+route
3 equally ranked IID candidates
TOCOPHEROLTOCOPHEROLR0ZB2556P8CREAM / TOPICALNAExact identifier — unii+route
3 equally ranked IID candidates
TOCOPHEROLTOCOPHEROLR0ZB2556P8CREAM / TOPICALNAExact 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
YELLOW WAXYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL20 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL20 %w/wExact identifier — unii+route+dosage form
3 equally ranked IID candidates
YELLOW WAXYELLOW WAX2ZA36H0S2VOINTMENT / TOPICAL20 %w/wExact identifier — unii+route+dosage form
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 Pain RelievingCAMPHOR, MENTHOL, METHYL SALICYLATEDLC Laboratories, Inc.5c3976da-a6cb-4b94-ae41-3e86b1ab13cb2026-07-28WarningsExact identifier
ndc (package): 24286-1554-2
ndc (package): 24286-1554-3
ndc (product): 24286-1554
ndc11 (package): 24286155403
ndc11 (package): 24286155402
spl id: 57b33b23-a8cc-8206-e063-6394a90ae0ac
spl set id: 5c3976da-a6cb-4b94-ae41-3e86b1ab13cb

Reported adverse events (FAERS/openFDA)#

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