COLD SORE FEVER BLISTER- docosanol cream 
H E B

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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 include:

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 2g (0.07 OZ)

*This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC, distributor of Abreva®.

*Docosanol Cream, 10% contains the only OTC medicine approved by the FDA to shorten healing time and duration of symptoms.

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

MADE WITH PRIDE AND CARE FOR H-E-B®,

SAN ANTONIO, TX 78204

Package label

Docosanol 10%

H-E-B Cold Sore Fever Blister Treatment

COLD SORE FEVER BLISTER 
docosanol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-661
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:37808-661-071 in 1 PACKAGE12/31/2023
12 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:37808-661-142 in 1 PACKAGE12/31/2023
22 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21238512/31/2023
Labeler - H E B (007924756)

Revised: 11/2023
Document Id: f6fbc45a-94c8-44e4-9941-af1df66d5ce4
Set id: 71b2bb18-4a48-42c2-b03a-dccf581a0d97
Version: 2
Effective Time: 20231107
 
H E B