Label: AHIST- chlorcyclizine hydrochloride tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 58407-025-01, 58407-025-06, 58407-025-30 - Packager: Magna Pharmaceutcals, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated August 17, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients (in each immediate-release tablet)
- Purpose
- Uses
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Warnings
Do not exceed recommended dosage.
Do not take this product unless directed by a doctor if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
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Directions
Do not exceed recommended dosage.
Adults and children 12 years of age and over: 1 tablet by mouth every 6-8 hours, not to exceed 3 tablets in 24 hours, or as directed by a doctor Children 6 to under 12 years of age: ½ tablet by mouth every 6-8 hours, not to exceed 1½ tablets in 24 hours, or as directed by a doctor Children under 6 years of age Consult a doctor - Inactive ingredients
- Questions or Comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 Tablet Carton
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INGREDIENTS AND APPEARANCE
AHIST
chlorcyclizine hydrochloride tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58407-025 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORCYCLIZINE HYDROCHLORIDE (UNII: NPB7A7874U) (CHLORCYCLIZINE - UNII:M26C4IP44P) CHLORCYCLIZINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) Product Characteristics Color green Score 2 pieces Shape OVAL Size 16mm Flavor Imprint Code AHIST;025 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58407-025-30 30 in 1 BOX 01/15/2013 1 NDC:58407-025-01 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:58407-025-06 6 in 1 BOX 01/31/2013 09/01/2019 2 NDC:58407-025-01 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 01/15/2013 Labeler - Magna Pharmaceutcals, Inc. (620988360)