Alahist Dm
fdaa062d-110e-798d-e053-6394a90a755c
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Description
ALAHIST DM LIQUID Drug Facts
Purpose
Antitussive Antihistamine Nasal Decongestant
Medication Information
Purpose
Antitussive
Antihistamine
Nasal Decongestant
Description
ALAHIST DM LIQUID Drug Facts
Uses
temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- runny nose
- sneezing
- itching of nose or throat
- itchy, watery eyes
- cough due to minor throat and bronchial irritation
- nasal congestion
- reduces swelling of nasal passages
Section 42229-5
ALAHIST DM LIQUID
Drug Facts
Warnings
Do not exceed recommended dosage.
Active Ing
(in each 5
mL
teaspoonful)
Dextromethorphan HBr............... 10 mg
Pheniramine Maleate.............. 12.5 mg
Phenylephrine HCl...................... 5 mg
Directions
Do not exceed recommended dosage.
| Adults and
children 12 years of age and over: |
2 teaspoonful (10 mL)
every 4 to 6 hours, not to exceed 12 teaspoonfuls in a 24 hours |
| Children 6 to
under 12 years of age: |
1 teaspoonful
(5 mL) every 4 to 6 hours, not to exceed 6 teaspoonfuls in 24 hours |
| Children under
6 years of age: |
Consult a doctor. |
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.
Other Information
Store at 59° - 86°F (15° - 30°C)
Inactive Ingredients
Citric Acid, Flavor, Methylparaben, Potassium Citrate, Propylene Glycol, Propylparaben, Purified water, Sucralose,Sorbitol
Questions? Comments?
Serious side effects associated with use of this product may be reported to this number.
Call 1-800-882-1041
Mon. - Fri. (8 a.m. to 5 p.m. CST).
Ask A Doctor Before Use
if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
- a cough that occurs with too much phlegm (mucus)
- heart disease
- high blood pressure
- thyroid disease
- diabetes
Principal Display Panel
When Using This Product
- excitability may occur, especially in children
- may cause marked drowsiness
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase the drowsiness effect
- be careful when driving a motor vehicle or operating machinery
If Pregnant Or Breast Feeding,
ask a health professional before use.
Keep Out of Reach of Children.
In case of overdose, get medical help or contact a Poison Control Center right away.
Ask A Doctor Or Pharmacist Before Use
if you are
taking sedatives or tranquilizers.
Structured Label Content
Uses
temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- runny nose
- sneezing
- itching of nose or throat
- itchy, watery eyes
- cough due to minor throat and bronchial irritation
- nasal congestion
- reduces swelling of nasal passages
Section 42229-5 (42229-5)
ALAHIST DM LIQUID
Drug Facts
Purpose
Antitussive
Antihistamine
Nasal Decongestant
Warnings
Do not exceed recommended dosage.
Active Ing (Active ing)
(in each 5
mL
teaspoonful)
Dextromethorphan HBr............... 10 mg
Pheniramine Maleate.............. 12.5 mg
Phenylephrine HCl...................... 5 mg
Directions
Do not exceed recommended dosage.
| Adults and
children 12 years of age and over: |
2 teaspoonful (10 mL)
every 4 to 6 hours, not to exceed 12 teaspoonfuls in a 24 hours |
| Children 6 to
under 12 years of age: |
1 teaspoonful
(5 mL) every 4 to 6 hours, not to exceed 6 teaspoonfuls in 24 hours |
| Children under
6 years of age: |
Consult a doctor. |
Do Not Use (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.
Other Information (Other information)
Store at 59° - 86°F (15° - 30°C)
Inactive Ingredients (Inactive ingredients)
Citric Acid, Flavor, Methylparaben, Potassium Citrate, Propylene Glycol, Propylparaben, Purified water, Sucralose,Sorbitol
Questions? Comments?
Serious side effects associated with use of this product may be reported to this number.
Call 1-800-882-1041
Mon. - Fri. (8 a.m. to 5 p.m. CST).
Ask A Doctor Before Use (Ask a doctor before use)
if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
- a cough that occurs with too much phlegm (mucus)
- heart disease
- high blood pressure
- thyroid disease
- diabetes
Principal Display Panel (PRINCIPAL DISPLAY PANEL)
When Using This Product (When using this product)
- excitability may occur, especially in children
- may cause marked drowsiness
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase the drowsiness effect
- be careful when driving a motor vehicle or operating machinery
If Pregnant Or Breast Feeding, (If pregnant or breast-feeding,)
ask a health professional before use.
Keep Out of Reach of Children. (Keep out of reach of children.)
In case of overdose, get medical help or contact a Poison Control Center right away.
Ask A Doctor Or Pharmacist Before Use (Ask a doctor or pharmacist before use)
if you are
taking sedatives or tranquilizers.
Advanced Ingredient Data
Raw Label Data
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Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:07:27.220921 · Updated: 2026-03-14T23:10:53.901398