Alahist LQ Liquid

ALAHIST LQ - diphenhydramine hydrochloride and phenylephrine hydrochloride liquid 
Poly Pharmaceuticals, Inc.

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Alahist LQ Liquid

Drug Facts

Active ingredients                      Purpose
(in each 5 mL teaspoonful)
                                                     Antihistamine
Diphenhydramine Hydrochloride.......... Antitussive
Phenylephrine Hydrochloride............Decongestant

Uses

temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other respiratory allergies:

Warnings

Do not exceed recommended dosage.

Do not use this product

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of the reach of children.

In case of accidental overdose seek professional help or contact a Poision Control Center immediately.

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and older:                    
1 teaspoonful (5 mL) every 4 to 6 hours, not to exceed 6 teaspoonfuls in 24 hours.
Children 6 to under 12 years of age:
1/2 teaspoonful (2.5 mL) every 4 to 6 hours, not to exceed 3 teaspoonfuls in 24 hours.
Children under 6 years of age:
Use is not recommended.

Other information

Store at 59o-86oF (15o-30oC)

Inactive ingredients


Citric Acid, Cotton Candy Flavor, Glycerin, Gum Fruit Flavor, Propylene Glycol,
Purified Water, Sodium Citrate, Sodium Saccharin, Sorbitol.

Questions? Comments?

Call 1-888-535-0305

PRODUCT PACKAGING

The packaging below represents the labeling currently used.

Principal Display Panel and Side Panel for 473mL Label:

NDC 50991-607-16

ALAHIST LQ LIQUID

Antihistamine / Antitussive / Decongestant

Each 5 mL (1 teaspoonful) contains:
Diphenhydramine HCl............. 25 mg
Phenylephrine HCl................. 7.5 mg

Fruit Candy Flavor

Dye Free - Sugar Free - Alcohol Free

Distributed by:
Poly Pharmaceuticals
Mobile, AL 36619

16 fl oz. (473 mL)

Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.

Dispense in a tight, light-resistant container with a child-resistant cap.

THIS BOTTLE NOT TO BE DISPENSED TO CONSUMER.

Manufactured by: Great Southern Laboratories, Houston, TX 77099

Distributed for: Poly Pharmaceuticals, Mobile, AL 36619

Iss. 02/09



Principal Display Panel and Side Panel for 15mL Label:

NDC 50991-607-15

ALAHIST LQ LIQUID

Antihistamine / Antitussive / Decongestant

Each 5 mL (1 teaspoonful) contains:
Diphenhydramine HCl............... 25 mg
Phenylephrine HCl................... 7.5 mg

Fruit Candy Flavor
Professional Sample: Not for sale
Dye Free - Sugar Free - Alcohol Free

1/2 fl oz (15 mL)

Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.

Supplied in a tight, light-resistant container with a child-resistant cap.

Manufactured by:
Great Southern Laboratories
Houston, TX 77099

Distributed for:
Poly Pharmaceuticals,
Mobile, AL 36619

Iss. 08/09

Alahist LQ Packaging
Alahist LQ Packaging
Alahist LQ Packaging
Alahist LQ Packaging
Alahist LQ Packaging


ALAHIST  LQ
diphenhydramine hydrochloride and phenylephrine hydrochloride   liquid
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)50991-607
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Diphenhydramine Hydrochloride (Diphenhydramine) Diphenhydramine Hydrochloride25 mg  in 5 mL
Phenylephrine Hydrochloride (Phenylephrine ) Phenylephrine Hydrochloride7.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found
Product Characteristics
Color    Score    
ShapeSize
FlavorFRUITImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
150991-607-1512 BOTTLE In 1 TRAYcontains a BOTTLE
115 mL In 1 BOTTLEThis package is contained within the TRAY (50991-607-15)
250991-607-16473 mL In 1 BOTTLENone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34112/20/2007

Labeler - Poly Pharmaceuticals, Inc. (198449894)
Registrant - Poly Pharmaceuticals (198449894)
Establishment
NameAddressID/FEIOperations
Great Southern Laboratories056139553manufacture
Revised: 09/2009Poly Pharmaceuticals, Inc.