Antiseptic Instant Pain Relief

Manufacturer
Pharma Nobis, LLC
Effective date
2023-12-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:05:33

Label at a glance#

ProductAntiseptic Instant Pain Relief
Active ingredientCAMPHOR (NATURAL), PHENOL
Label structure15 sections

Indications and uses

Helps prevent infection and temporarily relieves pain and itching in minor burns, cuts, insect bites, scrapes, sunburn and other minor skin irritations.

Dosage and administration

Adult and children 2 yrs and older: apply to affected area 1 to 3 times daily. Children under 2 yrs of age: Consult a doctor before use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 10.8%, Phenol 4.7 %

Purpose

OTC - PURPOSE SECTION

Pain Reliever, Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Helps prevent infection and temporarily relieves pain and itching in minor burns, cuts, insect bites, scrapes, sunburn and other minor skin irritations.

Warnings:

WARNINGS SECTION

For External Use Only. Do not induce vomiting. If vomiting occurs give fluids again. Do not use in or near the eyes: In case of eye contact, flush eyes with running water for 15 minutes, get medical attention immediately. Do not use on: deep punture wounds, animal bites, serious burns.

When using this product:

OTC - WHEN USING SECTION

Do not bandage. Do not use over large areas of the body.

Stop use and consult a doctor if:

OTC - STOP USE SECTION

Condition worsens. Symptoms last more than 7 days or clear up and occur again in a few days.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adult and children 2 yrs and older: apply to affected area 1 to 3 times daily.

Children under 2 yrs of age: Consult a doctor before use.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Citric acid, Eucalyptus Oil, Light Mineral Oil

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEBHEB

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vida MiaVida Mia

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Quality ChoiceQuality Choice

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DDMDDM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308940camphor 10.8 % / phenol 4.7 % Topical SolutionPSN2
308940camphor 108 MG/ML / phenol 47 MG/ML Topical SolutionSCD2
308940camphor 10.8 % / phenol 4.7 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82645-902-05Antiseptic Instant Pain Relief45 mL in 1 BOTTLE, GLASSLIQUID452

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82645-902ANTISEPTIC INSTANT PAIN RELIEF (CAMPHOR 10.8% AND PHENOL 4.7%) LIQUID [PHARMA NOBIS, LLC]2Current NDC, 1 package rows20231223_e42f484d-a642-3489-e053-2a95a90a4254.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82645-90282645-902-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Antiseptic Instant Pain ReliefCAMPHOR 10.8% AND PHENOL 4.7%Pharma Nobis, LLCe42f484d-a642-3489-e053-2a95a90a42542023-12-22WarningsExact identifier
ndc (package): 82645-902-05
ndc (product): 82645-902
ndc11 (package): 82645090205
spl id: 0d1cd55e-cd94-6e7e-e063-6294a90ae7a5
spl set id: e42f484d-a642-3489-e053-2a95a90a4254

Reported adverse events (FAERS/openFDA)#

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