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

----------

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:59726-922
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:59726-922-142 in 1 PACKAGE07/15/2023
12 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:59726-922-071 in 1 BOTTLE, PUMP07/15/2023
22 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20875407/15/2023
Labeler - P & L Development, LLC (800014821)

Revised: 8/2023
Document Id: e3ca66e1-8d74-4cc1-8658-fe4cf8c54c0f
Set id: 20d2480b-44b5-499f-8670-01d6a4e4cb34
Version: 2
Effective Time: 20230810
 
P & L Development, LLC