Label: ZILACTIN EARLY RELIEF COLD SORE- benzyl alcohol gel
- NDC Code(s): 50486-468-02
- Packager: Blairex Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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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
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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 THYMOL (UNII: 3J50XA376E) MENTHOL (UNII: L7T10EIP3A) TANNIC ACID (UNII: 28F9E0DJY6) WATER (UNII: 059QF0KO0R) BORIC ACID (UNII: R57ZHV85D4) HYDROXYPROPYL CELLULOSE (TYPE M) (UNII: U3JF91U133) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SALICYLIC ACID (UNII: O414PZ4LPZ) ALCOHOL (UNII: 3K9958V90M) EUCALYPTOL (UNII: RV6J6604TK) 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 Drug M022 06/30/2005 Labeler - Blairex Laboratories, Inc. (092575133)