FDA.reportPublic FDA data

Aftertest Pain Relief

Manufacturer
Diabetic Supply of Suncoast, Inc.
Effective date
2021-11-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:18

Label at a glance#

ProductAftertest Pain Relief
Active ingredientBENZOCAINE
Label structure11 sections

Indications and uses

Temporarily relieves pain and itching, associated with: minor cuts, scrapes, minor burns, insect bites.

Dosage and administration

When practical, cleanse affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product. Apply externally to the affected area up to 6 times daily.

Storage and handling

Store at room temperature 15-30 degrees C (59-86 degrees F). Do not freeze. Throw away any unused medicine after the expiration date.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine (10%)

Purpose

OTC - PURPOSE SECTION

Pain Reliever

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves pain and itching, associated with: minor cuts, scrapes, minor burns, insect bites.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use otherwise than as directed. Do not use if known sensitivity to product.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

SPL UNCLASSIFIED SECTION

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes or mouth.

Stop use and ask a doctor

OTC - STOP USE SECTION

If condition worsens, or symptoms persists for more than 7 days, symptoms do not get better, or if redness, irritation, swelling, pain or other symptoms occur or increase.

Directions

DOSAGE & ADMINISTRATION SECTION

When practical, cleanse affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product. Apply externally to the affected area up to 6 times daily.

OTC - ASK DOCTOR SECTION

Children Under 12 Years: Ask a doctor.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Alcohol Denat., Amica Montana Flower Extract, Diisopropyl Adipate, Eucalyptus Globulus Leaf Oil, Glycerin, Glycery Laurate, Menthol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Potassium Laurate, Propanediol, Propylene Glycol, Propylene Glycol Dilaurate, Propylene Glycol Monolaurate, Water.

STORAGE AND HANDLING SECTION

Store at room temperature 15-30 degrees C (59-86 degrees F). Do not freeze.

Throw away any unused medicine after the expiration date.

OTC - QUESTIONS SECTION

Questions or Comments, 24/7
Toll-free: 1-866-373-2824

PRINCIPAL DISPLAY PANEL - 4 ml Applicator Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aftertest

TOPICAL
PAIN

relief stick

Formulated for use with
lancets and syringes

Soothes & Protects
after
puncture

Active Ingredients:
Benzocaine (10%)

Container:
4ml/0.135 fl oz

* Never use before
testing or injection.
Use only after
puncture.

ADVOCATE ® DIABETES

PRINCIPAL DISPLAY PANEL - 4 ml Applicator Carton
PRINCIPAL DISPLAY PANEL - 4 ml Applicator Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71814-410-012021-11-04C16284748780-19d75b9d0-e428-f424-e053-dadaa90a57ceAftertest Pain Relief
71814-410-012020-01-31C16284748780-19d75b9d0-e428-f424-e053-dadaa90a57ceAftertest Pain Relief

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71814-410-01ML - Milliliter71814-410b7728e13-e98a-4972-99d0-a4f434f6dce712017-12-14

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71814-41071814-410-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL LAURATEY98611C087IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
POLYSORBATE 207T1F30V5YHIACT
POTASSIUM LAURATEV4361R8N4ZIACT
PROPANEDIOL5965N8W85TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPYLENE GLYCOL DILAURATERMY7XGC3LVIACT
PROPYLENE GLYCOL MONOLAURATE668Z5835Z3IACT
WATER059QF0KO0RIACT
BENZOCAINEU3RSY48JW5ACTIB

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
f05a1679-1319-7e73-e053-2a95a90a905a1469366a-5e93-4a2c-96b6-425b1cc7b2d92022-12-21WarningsExact identifier
spl set id: 1469366a-5e93-4a2c-96b6-425b1cc7b2d9

Reported adverse events (FAERS/openFDA)#

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