- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
-
Warnings
Stop use and ask a physician if
- sore mouth symptoms do not improve in 7 days
- condition worsens or symptoms clear up and occur again within a few days
- swelling, rash or fever develops
- irritation, pain or redness persists or worsens
- apply only to affected area
- do not exceed recommended dosage
- avoid contact with the eyes
- do not use for more than 7 days unless directed by a physician or dentist
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ZILACTIN EARLY RELIEF COLD SORE
benzyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50486-468 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzyl alcohol (UNII: LKG8494WBH) (benzyl alcohol - UNII:LKG8494WBH) benzyl alcohol 0.1 g in 1 g Inactive Ingredients Ingredient Name Strength boric acid (UNII: R57ZHV85D4) Hydroxypropyl Cellulose (Type M) (UNII: U3JF91U133) propylene glycol (UNII: 6DC9Q167V3) salicylic acid (UNII: O414PZ4LPZ) alcohol (UNII: 3K9958V90M) eucalyptol (UNII: RV6J6604TK) thymol (UNII: 3J50XA376E) menthol (UNII: L7T10EIP3A) tannic acid (UNII: 28F9E0DJY6) water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50486-468-02 1 in 1 CARTON 06/30/2005 1 7.1 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 OTC monograph not final part356 06/30/2005 Labeler - Blairex Laboratories, Inc. (092575133)