Label: DOCOSANOL cream
- NDC Code(s): 51316-763-02, 51316-763-04, 51316-763-64
- Packager: CVS Pharmacy, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 18, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
-
Warnings
This product may cause a severe allergic reaction. Symptoms may include:
- hives
- facial swelling
- wheezing/difficulty breathing
- shock
- rash
If an allergic reaction occurs, stop use and seek medical help right away.
For external use only
Do not use
- if you are allergic to any ingredient in this product
- apply only to the affected areas
- do not use in or near the eyes
- avoid applying directly inside your mouth
- do not share this product with anyone. This may spread the infection.
- your cold sore gets worse or the cold sore is not healed within 10 days
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
- adults and children 12 years or over:
• wash hands before and after applying cream
• apply to affected area on face or lips at the first sign of cold sore/fever blister (tingle)
• early treatment ensures the best results
• rub in gently but completely
• use 5 times a day until healed
- children under 12 years: ask a doctor
- Other information
- Inactive ingredient
- Questions or Comments?
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
-
PRINCIPAL DISPLAY PANEL
NDC 51316-763-64
Docosanol Cream, 10%
Compare to the active ingredient in Abreva®*
Cold Sore/Fever Blister Treatment
Non-prescription Medicine to Shorten Healing Time**
Cold Sore Treatment
For Topical Use Only
NET WT 2g (0.07 oz)
*This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Abreva®.
**Contains the only non-prescription cold sore medicine approved by the FDA to shorten healing time and duration of symptoms.
RETAIN THIS INSERT FOR FULL PRODUCT USES, DIRECTIONS AND WARNINGS
Distributed by:
CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2023 CVS/Pharmacy
CVS.com® 1-800-SHOP CVS V-38892
Made in India.
Mfg. License No.: G/25/2216
TUBE PACK
NDC 51316-763-04
Docosanol Cream, 10%
Compare to the active ingredient in Abreva®*
Cold Sore/Fever Blister Treatment
Non-prescription Medicine to Shorten Healing Time**
Cold Sore Treatment
For Topical Use Only
NET WT 2g (0.07 oz)
*This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Abreva®.
**Contains the only non-prescription cold sore medicine approved by the FDA to shorten healing time and duration of symptoms.
RETAIN THIS INSERT FOR FULL PRODUCT USES, DIRECTIONS AND WARNINGS
Distributed by:
CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2023 CVS/Pharmacy
CVS.com® 1-800-SHOP CVS V-38892
Made in India.
Mfg. License No.: G/25/2216
TUBE PACK
NDC 51316-763-02
Docosanol Cream, 10%
Compare to the active ingredient in Abreva®*
Cold Sore/Fever Blister Treatment
Non-prescription Medicine to Shorten Healing Time**
Cold Sore Treatment
For Topical Use Only
NET WT 2g (0.07 oz)
*This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Abreva®.
**Contains the only non-prescription cold sore medicine approved by the FDA to shorten healing time and duration of symptoms.
RETAIN THIS INSERT FOR FULL PRODUCT USES, DIRECTIONS AND WARNINGS
Distributed by:
CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2023 CVS/Pharmacy
CVS.com® 1-800-SHOP CVS V-38892
Made in India.
Mfg. License No.: G/25/2216
-
INGREDIENTS AND APPEARANCE
DOCOSANOL
docosanol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-763 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOCOSANOL (UNII: 9G1OE216XY) (DOCOSANOL - UNII:9G1OE216XY) DOCOSANOL 100 mg in 1 g Inactive Ingredients Ingredient Name Strength 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 Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-763-04 1 in 1 PACKAGE 01/06/2023 1 2 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:51316-763-64 1 in 1 PACKAGE 01/06/2023 2 2 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 3 NDC:51316-763-02 1 in 1 PACKAGE 01/06/2023 3 2 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA215839 01/06/2023 Labeler - CVS Pharmacy, Inc. (062312574) Registrant - Alembic Pharmaceuticals Limited (650574663) Establishment Name Address ID/FEI Business Operations Contract Packaging Resources, Inc. 960203917 PACK(51316-763) Establishment Name Address ID/FEI Business Operations Alembic Pharmaceuticals Limited 871411532 MANUFACTURE(51316-763) , ANALYSIS(51316-763)