Amish Origins Topical Analgesic Ointment Camphor 2%

Manufacturer
Amish Origins Management, LLC
Effective date
2024-02-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:18

Label at a glance#

ProductAmish Origins Topical Analgesic Camphor 2%
Active ingredientCAMPHOR (SYNTHETIC)
Label structure8 sections

Indications and uses

For the temporary relief of pain and itching associated with minor burns, sunburn, minor, cuts, scrapes, insect bites, minor skin irritations, and rashes due to poison ivy.

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 2%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

  • For the temporary relief of pain and itching associated with minor burns, sunburn, minor, cuts, scrapes, insect bites, minor skin irritations, and rashes due to poison ivy.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical helpor contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: do not use, consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Bees Wax, Chickweed, Comfrey, Eucalyptus Oil, Lavender Oil, Olive Oil, Pine Oil, Plantain, Wintergreen Oil

Questions or comments?

OTC - QUESTIONS SECTION

1-888-530-7643

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Label01Outer Label01Inner label01Inner label01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2675876camphor 2 % Topical OintmentPSN1
2675876camphor 0.02 MG/MG Topical OintmentSCD1
2675876camphor 2 % Topical OintmentSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62212-003-01Amish Origins Topical Analgesic Camphor 2%57 g in 1 CONTAINERSALVE571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62212-003AMISH ORIGINS TOPICAL ANALGESIC CAMPHOR 2% (CAMPHOR (SYNTHETIC)) SALVE [AMISH ORIGINS MANAGEMENT, LLC]1Current NDC, 1 package rows20240302_ffe15aed-ea90-4db8-aace-d691a81c05ae.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
62212-00362212-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Amish Origins Topical Analgesic Camphor 2%CAMPHOR (SYNTHETIC)Amish Origins Management, LLCffe15aed-ea90-4db8-aace-d691a81c05ae2024-02-29WarningsExact identifier
ndc (package): 62212-003-01
ndc (product): 62212-003
ndc11 (package): 62212000301
spl id: 12887bc8-16ff-9683-e063-6294a90aee55
spl set id: ffe15aed-ea90-4db8-aace-d691a81c05ae

Reported adverse events (FAERS/openFDA)#

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