Label: CHLORESIN- acetaminophen, dextromethorphan, guaifenesin, phenylephrine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 51532-0107-2 - Packager: Affasco Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 21, 2019
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings:
Liver Warning:
This product contains acetaminophen. Severe liver damage may occur if you take more than 8 tablets in 24 hours, if you take with other drugs containing acetaminophen (prescription or nonprescription), or if you have 3 or more alcoholic drinks every day while using this product.
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- OVERDOSAGE
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CHLORESIN
acetaminophen, dextromethorphan, guaifenesin, phenylephrine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51532-0107 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE 5 Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) STEARIC ACID (UNII: 4ELV7Z65AP) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score no score Shape ROUND Size 12mm Flavor Imprint Code FR12 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51532-0107-2 2 in 1 PACKET; Type 0: Not a Combination Product 10/25/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 10/25/2016 Labeler - Affasco Inc. (609982723) Registrant - ULTRAtab laboratories, Inc. (151051757) Establishment Name Address ID/FEI Business Operations ULTRA SEAL CORPORATION 085752004 pack(51532-0107) Establishment Name Address ID/FEI Business Operations ULTRAtab LABORATORIES, INC. 151051757 manufacture(51532-0107)