Label: PUBLIX SORE THROAT FAST RELIEF ORAL ANESTHETIC- phenol spray
- NDC Code(s): 41415-703-06
- Packager: PUBLIX SUPER MARKETS, INC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 7, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
Sore Throat Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious.
Consult doctor promptly. Do not use more than 2 days or administer to children under 6 years of age unless directed by doctor.
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Directions
- Adults and children 12 years of age and older:
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- Apply to the affected area (one spray). Allow to remain in place for at least 15 seconds, then spit out
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- Use every 2 hours or as directed by a doctor or dentist
- Children 6 years to 12 years of age should be supervised in the use of this product
- Children under 6 years: consult a doctor or dentist
- Other information
- Inactive ingredients
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Principal Display Panel
*Compare to active ingredient in Chloraseptic®*
Sore Throat Spray
Phenol/ Oral Pain Reliever
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- Fast acting
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- Numbs on Contact
- SUGAR-FREE
- ASPIRIN-FREE
NATURALLY CHERRY FLAVOR
6 FL OZ (177 mL)
*This product is not manufactured or distributed by Medtech Products Inc., a Prestige Brands Co., distributor of Chloraseptic®
TAMPER-EVIDENT: DO NOT USE IF IMPRINTED SHRINK BAND IS BROKEN OR MISSING.
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INGREDIENTS AND APPEARANCE
PUBLIX SORE THROAT FAST RELIEF ORAL ANESTHETIC
phenol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41415-703 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL 1.4 g in 100 mL Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color RED Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41415-703-06 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 10/24/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 10/24/2022 Labeler - PUBLIX SUPER MARKETS, INC (006922009)