SierraSil Pain Relief

Manufacturer
D&d Essential Oils, Llc. | D&d Essential Oils, Llc.,
Effective date
2018-10-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:57:01

Label at a glance#

ProductSierraSil Pain Relief
Active ingredientCAMPHOR (NATURAL)
Label structure10 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Dosage and administration

adults and children 2 yrs of age and older: apply to affected area not more than 3 to 4 times daily. children under 2 yrs of age: consult a doctor.

Storage and handling

shake well before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.1%

Purpose

OTC - PURPOSE SECTION

Camphor 3.1%.........................................Topical analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

WARNINGS SECTION

For external use only.

Do not

OTC - DO NOT USE SECTION

  • apply to wounds or damaged skin
  • bandage tightly
  • use with a heating pad

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes or mucous membranes
  • use only as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTHER SAFETY INFORMATION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 yrs of age and older: apply to affected area not more than 3 to 4 times daily.
  • children under 2 yrs of age: consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

  • shake well before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Eucalyptus Globulus Leaf Oil, Hydrothermal Mineral Complex (SierraSil), Lavandula Angustifolia (Lavender) Oil, Mentha arvensis (Peppermint) Oil, Rosmarinus Officinalis Leaf (Rosemary) Oil

Questions?

OTC - QUESTIONS SECTION

Visit www.sierrasil.com or call toll free 1-877-743-7720 Monday-Friday 8:00am to 4:30pm

DESCRIPTION SECTION

Distributed by SierraSil Health Inc.

1500 NW Bethany Blvd Suite 200,

Beaverton, OR, 97006

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SierraSil

Pain

Relief

TOPICAL

ANALGESIC

SPRAY

TEMPORARILY

RELIEVES

MINOR ACHES

AND PAINS

1 fl oz / 30 mL

SierrasilcartonSierrasilcarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046527camphor 3.1 % Topical SprayPSN1
1424351Sierrasil Pain Relief 3.1 % Topical SprayPSN1
1424351camphor 31 MG/ML Topical Spray [Sierrasil Pain Relief]SBD1
1046527camphor 31 MG/ML Topical SpraySCD1
1046527camphor 3.1 % Topical SpraySY1
1424351Sierrasil Pain Relief 3.1 % Topical SpraySY1
1424351Sierrasil Pain Relief 31 MG/ML Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72608-002-302022-01-28C16284748780-1d6a99b39-9d38-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72608-002-30SierraSil Pain Relief1 in 1 CARTONSPRAY11
72608-002-30SierraSil Pain Relief30 mL in 1 BOTTLE, SPRAYSPRAY301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72608-002SIERRASIL PAIN RELIEF (CAMPHOR) SPRAY [D&D ESSENTIAL OILS, LLC.]1Legacy NDC, 2 package rows20181015_78357755-255d-1030-e053-2991aa0aaa04.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72608-00272608-002-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
78357755-255e-1030-e053-2991aa0aaa0478357755-255d-1030-e053-2991aa0aaa042018-10-14WarningsExact identifier
spl id: 78357755-255e-1030-e053-2991aa0aaa04
spl set id: 78357755-255d-1030-e053-2991aa0aaa04

Reported adverse events (FAERS/openFDA)#

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