Label: SORE THROAT CHERRY- phenol spray
- NDC Code(s): 63868-811-55
- Packager: QUALITY CHOICE (Chain Drug Marketing Association)
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 1, 2024
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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 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
- apply to affected area
- use every 2 hours
- allow to remain in place for at least 15 seconds, then spit out
age dose adults and children 12 years and over for each application, spray 5 times children 3 to 11 years should be supervised in use of this product for each application, spray 3 times children under 3 years ask a doctor or dentist - Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
*Compare to the Active Ingredient in Chloraseptic®
Sore Throat Spray
Oral anesthetic/analgesic
Phenol
Fast acting/long lasting
Alcohol 0.10%
Cherry flavor
FL OZ (mL)
*This product is not manufactured or distributed by Prestige Brands Inc., distributor of Chloraseptic®.
TAMPER EVIDENT: DO NOT USE F IMPRINTED WRAP AROUND THE CAP IS BROKEN OR TORN.
Distributed by C.D.M.A., Inc.©
43157 W. Nine Mile
Novi, MI 48376-0995
- Package Label
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INGREDIENTS AND APPEARANCE
SORE THROAT CHERRY
phenol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-811 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:63868-811-55 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/31/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 08/31/2014 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)