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Drug Facts
Distributed by:
Glendale Inc
Villa Park, IL 60181
Glenmax Peb
FDA Label NDC 70147-222
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Glendale Inc for the product Glenmax Peb (NDC 70147-222). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, otc - purpose, uses, warnings, otc - do not use, otc - ask doctor, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
| Active ingredients (in each teaspoonful) | Purpose |
|---|---|
| Brompheniramine Maleate 4 mg | Antihistamine |
| Phenylephrine Hydrochloride 10 mg | Nasal Decongestant |
Uses
temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:
- runny nose
- sneezing
- itching of the nose or throat
- itchy, watery eyes
- nasal congestion
- temporarily restores freer breathing through the nose
- reduces swelling of nasal passages
Warnings
Do not exceed recommended dosage.
Otc - Do Not Use
Do not use this product
- to sedate a child or make a child sleepy
- 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.
Otc - Ask Doctor
Ask a doctor before use if you have
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a breathing problem such as emphysema or chronic bronchitis
Otc - Ask Doctor/Pharmacist
Ask a doctor or pharmacist before use if you are
- taking any other nasal decongestant or stimulant
- taking sedatives or tranquilizers
Otc - When Using
When using this product
- marked drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
- excitability may occur, especially in children
Otc - Stop Use
Stop use and ask a doctor if
- nervousness, dizziness, or sleeplessness occur
- cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. These could be signs of a serious condition.
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding, ask a health professional before use.
Otc - 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.
Directions
Do not exceed 6 dosage in a 24-hour period.
| Adults and children 12 years of age and over: | 1 teaspoonful every 4 hours |
| Children under 12 years of age: | Consult a physician |
Other Information
Store at 59°-86°F (15°-30°C) [see USP for Controlled Room Temperature]
Inactive Ingredients
Fruit gum flavor, citric acid, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol.
Questions? Comments?
To report a serious adverse event or obtain product information, Call 1-630-530-7000.
Principal Display Panel - 473 Ml Bottle Label
NDC 70147-0222-16
Glenmax
PEB
Antihistamine
Nasal Decongestant
Each teaspoonful for oral
administration contains:
Brompheniramine Maleate
4 mg
Phenylephrine HCl
10 mg
SUGAR FREE / DYE FREE
ALCOHOL FREE
Fruit Gum Flavored Liquid
Tamper evident by foil seal under cap.
Do not use if foil seal is broken or missing.
Distributed by:
Glendale Inc
Villa Park, IL 60181
16 fl oz. (473 mL)
Principal Display Panel (473 mL Bottle Label)
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