Label: SORE THROAT- phenol spray
- NDC Code(s): 21130-376-06
- Packager: Safeway, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 15, 2024
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- 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 a doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a doctor.
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Directions
- adults and children 6 years of age and older
- apply to affected area (one spray)
- allow to remain in place for at least 15 seconds, then spit out
- use every 2 hours as directed by a doctor or dentist
- children under 12 years of age should be supervised in the used in this product
- children under 6 years of age, consult a doctor or dentist
- adults and children 6 years of age and older
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to Chloraseptic® active ingredient*
Sore Throat Spray
PHENOL 1.4 %
Oral Anesthetic / Analgesic
CHERRY FLAVOR
- Alcohol 0.10%
- Aspirin free
- SUGAR FREE
FL OZ (mL)
*This product is not manufactured or distributed by Prestige Brands Inc., distributor of Chloraseptic®.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND CAP IS BROKEN OR MISSING.
DISTRIBUTED BY
BETTER LIVING BRAND LLC
P.O. BOX 99, PLEASANTON, CA 94566-0009
- Package Label
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INGREDIENTS AND APPEARANCE
SORE THROAT
phenol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-376 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 ALCOHOL (UNII: 3K9958V90M) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-376-06 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/30/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 11/30/2014 Labeler - Safeway, Inc. (009137209)