Label: ALAHIST D- pheniramine maleate, phenylephrine hcl tablet
- NDC Code(s): 50991-776-01, 50991-776-02
- Packager: Poly Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 27, 2024
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- ACTIVE INGREDIENT
- USES
-
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.Ask a doctor before use ifyou have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- trouble urinating due to enlargement of the prostate gland
- heart disease
- high blood pressure
- thyroid disease
- diabetes
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
When using this product
- excitability may occur, especially in children
- may cause drowsiness
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase the drowsiness effect
- use caution when driving a motor vehicle or operating machinery
Stop use and ask a doctor if
nervousness, dizziness, or sleeplessness occur
symptoms do not improve within 7 days or are accompanied by feverIf pregnant or breast-feeding, ask a health
professional before use. - DIRECTIONS
- INACTIVE INGREDIENTS
- QUESTIONS
- OTHER INFORMATION
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- Package Label
-
INGREDIENTS AND APPEARANCE
ALAHIST D
pheniramine maleate, phenylephrine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50991-776 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENIRAMINE MALEATE (UNII: NYW905655B) (PHENIRAMINE - UNII:134FM9ZZ6M) PHENIRAMINE MALEATE 17.5 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) Product Characteristics Color yellow Score 2 pieces Shape OVAL Size 11mm Flavor Imprint Code A;D Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50991-776-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 2 NDC:50991-776-02 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 04/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2020 Labeler - Poly Pharmaceuticals, Inc. (198449894)