O24 Pain Neutralizer

Manufacturer
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#

ProductO24 Pain Neutralizer
Active ingredientCAMPHOR (NATURAL)
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.1%

OTC - PURPOSE SECTION

Camphor 3.1%.............................External Analgesic

INDICATIONS & USAGE SECTION

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

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

WARNINGS SECTION

For External Use Only.

OTC - DO NOT USE SECTION

Do Not Use

  • For arthritis-like conditions in children under 2.
  • on wounds, damaged, broken or irritated skin.

OTC - WHEN USING SECTION

When Using This Product

  • use only as directed.
  • do not bandage tightly.
  • avoid contact with the eyes and mucous membranes.

OTC - STOP USE SECTION

Stop Use and Ask Doctor If

  • condition worsens
  • symptoms last more than 7 days
  • symptoms clear up and come back in a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and older: apply to (gently wipe) affected area not more than 3 to 4 times daily
  • children under 2 years of age: consult a physician

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Eucalyptus Globulus Leaf Oil, Mentha arvensis (Peppermint Leaf) Oil, Rosmarinus Ofcinalis Leaf (Rosemary) Oil

DESCRIPTION SECTION

Distributed by

O24 TM Naturals, LLC

306 Hallmark Dr.,

Arlington, TX 76011

Questions?

Call TOLL-FREE:

1.866.902.8594 or visit us at:

www.O24zone.com

O24 TM is a Registered Trademark

of O24 TM Naturals, LLC.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

024 TM Naturals

024 TM

Pain Neutralizer

Topical Analgesic

Penetrating Pain Relief

for the temporary relieft of minor aches & pains associated with arthritis, strains, backaches, and bruises

10 Towelettes

(4 in x 6 in / 10.2 cm x 15.2 cm)

O24TowelettesO24Towelettes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72608-004-102022-01-28C16284748780-1d6a99b39-ea50-a426-e053-dadaa90af4c278357755-2570-1030-e053-2991aa0aaa04

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72608-004-10O24 Pain Neutralizer2 g in 1 PACKETLIQUID21
72608-004-10O24 Pain Neutralizer10 in 1 CARTONLIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72608-004O24 PAIN NEUTRALIZER (CAMPHOR) LIQUID [D&D ESSENTIAL OILS, LLC.,]1Legacy NDC, 2 package rows20181015_78357755-2570-1030-e053-2991aa0aaa04.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
72608-00472608-004-10

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
78357755-2571-1030-e053-2991aa0aaa0478357755-2570-1030-e053-2991aa0aaa042018-10-14WarningsExact identifier
spl id: 78357755-2571-1030-e053-2991aa0aaa04
spl set id: 78357755-2570-1030-e053-2991aa0aaa04

Reported adverse events (FAERS/openFDA)#

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