Label: SORE THROAT CHERRY- phenol spray
- NDC Code(s): 41163-376-06
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 13, 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 that occurs with high fever, headache, nausea, and vomiting may be serious. Ask a doctor right away. Do not use more than 2 days or give to children under 3 years of age.
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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, than spit out
- use every 2 hours as directed by a doctor or dentist
- children under 12 years of age should be supervised in the use of 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
Relieves Sore Throat
ALCOHOL 0.10%
ASPIRIN FREE
SUGAR FREE
Cherry Flavor
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 SUPERVALU INC.
EDEN PRAIRIE, MN 95344 USA
supervaluprivatebrands.com
- Package Label
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INGREDIENTS AND APPEARANCE
SORE THROAT CHERRY
phenol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-376 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 red Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-376-06 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/30/2018 12/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 04/30/2018 12/31/2024 Labeler - United Natural Foods, Inc. dba UNFI (943556183)