AFTERTEST PAIN RELIEF- benzocaine stick

Aftertest Pain Relief by

Drug Labeling and Warnings

Aftertest Pain Relief by is a Otc medication manufactured, distributed, or labeled by Diabetic Supply of Suncoast, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzocaine (10%)

Purpose

Pain Reliever

Uses

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

Warnings

For external use only.

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

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

Keep out of reach of children.

Flammable. Keep away from heat and flame.

When using this product

Avoid contact with eyes or mouth.

Stop use and ask a doctor

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

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.

ASK DOCTOR

Children Under 12 Years: Ask a doctor.

Inactive Ingredient

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

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

Throw away any unused medicine after the expiration date.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL - 4 ml Applicator Carton

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

INGREDIENTS AND APPEARANCE

AFTERTEST PAIN RELIEF 
benzocaine stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71814-410
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5)	Benzocaine	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)
Arnica Montana Flower (UNII: OZ0E5Y15PZ)
Diisopropyl Adipate (UNII: P7E6YFV72X)
Eucalyptus Oil (UNII: 2R04ONI662)
Glycerin (UNII: PDC6A3C0OX)
Glyceryl Laurate (UNII: Y98611C087)
Menthol, Unspecified Form (UNII: L7T10EIP3A)
Polysorbate 20 (UNII: 7T1F30V5YH)
Potassium Laurate (UNII: V4361R8N4Z)
Propanediol (UNII: 5965N8W85T)
Propylene Glycol (UNII: 6DC9Q167V3)
Propylene Glycol Dilaurate (UNII: RMY7XGC3LV)
Propylene Glycol Monolaurate (UNII: 668Z5835Z3)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71814-410-01	1 in 1 CARTON	01/28/2017
1		4 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part348	01/28/2017

Labeler - Diabetic Supply of Suncoast, Inc. (043081723)