COLD SORE TREATMENT- docosanol cream 
P & L Development, LLC

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Docosanol Cream, 10%

Active ingredient

 Docosanol  10%

Purpose

Cold sore/fever blister treatment

Uses

Warnings

Allergy Alert: This product may cause a severe allergic reaction. Symptoms may cause:

if an allergic reaction occurs, stop use and seek medical help right away.

For External use only

Do not use

When using this product

Stop use and ask a doctor if

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

benzyl alcohol, light mineral oil, propylene glycol, purified water, sucrose distearate, sucrose stearate

Questions or Comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal display panel

†Compare to active ingredient in Abreva®

docosanol cream 10%

cold sore/fever blister treatment

NET WT

g (oz)

*Non-prescription cold sore medicine to shorten healing time and duration of symptoms.

†This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Abreva®

RETAIN THIS INSERT FOR FULL PRODUCT USES, DIRECTIONS AND WARNINGS.

Distributed by: PL Developments

200 Hicks Street, Westbury, NY 11590

Package Label

Docosanol 10%

WELLNESS BASICS Cold Sore Fever Blister Treatment

COLD SORE TREATMENT 
docosanol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59726-924
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCOSANOL (UNII: 9G1OE216XY) (DOCOSANOL - UNII:9G1OE216XY) DOCOSANOL100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SUCROSE DISTEARATE (UNII: 33X4X4B90S)  
SUCROSE STEARATE (UNII: 274KW0O50M)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59726-924-071 in 1 PACKAGE05/28/2021
12 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20875405/28/2021
Labeler - P & L Development, LLC (800014821)

Revised: 10/2022
Document Id: 3a93fdcf-bd3a-48ed-9821-48947cc2ac2a
Set id: 15d1a6c5-4a61-48f3-b45e-a7e34cbeb294
Version: 2
Effective Time: 20221018
 
P & L Development, LLC