Indications and uses
Treat cold sores / fever blisters Help guard against infection
Treat cold sores / fever blisters Help guard against infection
Adults and children over 2 years of age: Clean the lip area of any lip preparations, lotions, ointments, residual beverages, or cosmetics including lipstick using warm water and a washcloth Remove the cardboard top from applicator and place onto the glass/plastic vial end - opposite the brush end of the product Squeeze the cardboard to break the inner glass vial open Saturate the applicator end with solution by ho...
Store at room temperature: 15° - 30° C (59° - 86° F) The ingredients in toothpaste, softdrinks, and some fruit juices can de-activate the active ingredient. For best results, avoid brushing your teeth with toothpaste or drinking soft drinks or fruit juices for one hour after applying.
For external use only. Flammable, keep away from fire or flame.
If swallowed, get medical help or contact a Poison Control Center right away.

CVS
pharmacy
NEW!
NDC 50730-2000-1
Compare to VIROXYN®
SINGLE APPLICATION
COLD SORE
TREATMENT
TREATS 2 COLD SORES
2 Vials
(0.6 ml)
1 Vial per treatment
CVS Quality Money Back Guarantee
US Patent No's 6,211,243B1 and 6,322,243 and 6,410,599 and 6,414,032 and 6,423,750 and 6,759,434
CVS/Pharmacy single application cold sore treatment uses a patented new approach to treating cold sores - rubbing the cold sore with the applicator tip delivers the germicidal medicine directly to the site of the infection.
Cold Sores and Fever Blisters are both caused by the Herpes Simples
virus (typically HSV-1) and are just different popular names for the
HSV-caused lesions.
©2009 CVS/pharmacy
www.cvs.com 1-800-shop-CVS

| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50730-2000-1 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-bdc0-621f-e053-dbdaa90a74ad | DRUG FACTS |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50730-2000-1 | Cold Sore Treatment | 0.6 mL in 1 VIAL, PATENT DELIVERY SYSTEM | TINCTURE | 0.6 | 1 | |
| 50730-2000-1 | Cold Sore Treatment | 2 in 1 PACKAGE | TINCTURE | 2 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50730-2000 | COLD SORE TREATMENT (BENZALKONIUM CHLORIDE) TINCTURE [H AND P INDUSTRIES, INC. DBA TRIAD GROUP] | 1 | Legacy NDC, 2 package rows | 20091211_3beb9bed-6bfd-4e6f-be1c-0ba166504803.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Benzalkonium chloride | ACTIVE INGREDIENT | F5UM2KM3W7 | 1 | |
| Benzalkonium | ACTIVE MOIETY | 7N6JUD5X6Y | 1 | |
| isopropyl alcohol | INACTIVE INGREDIENT | ND2M416302 | 1 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 50730-2000 | 50730-2000-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Benzalkonium chloride | F5UM2KM3W7 | ACTIB |
| isopropyl alcohol | ND2M416302 | IACT |
| water | 059QF0KO0R | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SOLUTION / TOPICAL | 40 %w/v | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | LOTION, AUGMENTED / TOPICAL | 2070 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SPONGE / TOPICAL | 4 %w/w | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | OIL / TOPICAL | 72 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | GEL / TOPICAL | 75 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | SWAB / TOPICAL | 43.9 %w/w | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | OIL / AURICULAR (OTIC) | 6 mg | ||
| isopropyl alcohol | ISOPROPYL ALCOHOL | ND2M416302 | GEL, METERED / TOPICAL | 525 mg |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 52ca50c3-5890-4f93-ab96-67b39ddb13dc | 3beb9bed-6bfd-4e6f-be1c-0ba166504803 | 2009-12-09 | Warnings | 52ca50c3-5890-4f93-ab96-67b39ddb13dc 3beb9bed-6bfd-4e6f-be1c-0ba166504803 |
Adverse event summaries are temporarily unavailable. Other product information remains available.