NDC | 0485-0240-01 |
Set ID | 07cd07a1-d84c-4a91-8fa6-5eb58dd23991 |
Category | HUMAN OTC DRUG LABEL |
Packager | EDWARDS PHARMACEUTICALS, INC. |
Generic Name | |
Product Class | alpha-1 Adrenergic Agonist |
Product Number | |
Application Number | PART341 |
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
- Do not exceed recommended dosage.
Do not use this product
- if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product
Do not use this product, unless directed by a doctor, if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- a persistent or chronic cough that occurs with too much phlegm (mucus)
- heart disease
- high blood pressure
- thyroid disease
- diabetes mellitus
- difficulty in urination due to enlargement of the prostate gland
Do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor.
When using this product
- excitability may occur, especially in children
- may cause marked drowsiness
- sedatives and tranquilizers may increase drowsiness effect
- avoid alcoholic beverages
- use caution when driving a motor vehicle or operating machinery
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Directions
Do not exceed recommended dosage.
Adults and children 12 years of age and over: 1 tablet every 4 hours, not to exceed 6 tablets in 24 hours, or as directed by a doctor Children 6 to under 12 years of age: 1/2 tablet every 4 hours, not to exceed 3 tablets in 24 hours, or as directed by a doctor Children under 6 years of age: Consult a doctor. - Inactive ingredients
- Questions or Comments?
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PRINCIPAL DISPLAY PANEL - 100 Tablet Bottle Label
NDC 0485-0240-01
ED A-HIST DM TABLETS
Antihistamine • Antitussive • Nasal Decongestant
Each tablet contains:
Chlorpheniramine Maleate 4 mg
Dextromethorphan HBr 10 mg
Phenylephrine HCl 10 mgStore at 59°-86°F (15°-30°C) [see USP Controlled Room Temperature].
Tamper evident by foil seal under cap.
Do not use if foil seal is broken or missing.Manufactured for:
EDWARDS
Pharmaceuticals, Inc.
Ripley, MS 38663100 tablets
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INGREDIENTS AND APPEARANCE
ED-A-HIST DM
chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0485-0240 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 4 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) Product Characteristics Color purple Score 2 pieces Shape OVAL Size 16mm Flavor Imprint Code ED;DM Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0485-0240-01 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/27/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 10/27/2014 Labeler - EDWARDS PHARMACEUTICALS, INC. (195118880)