Aller-Chlor by Rugby Laboratories, Inc. / Hi-Tech Pharmacal Co., Inc. Drug Facts

Aller-Chlor by

Drug Labeling and Warnings

Aller-Chlor by is a Otc medication manufactured, distributed, or labeled by Rugby Laboratories, Inc., Hi-Tech Pharmacal Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLER-CHLOR- chlorpheniramine maleate syrup 
Rugby Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient (in each 5mL teaspoonful)

Chlorpheniramine Maleate 2 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms of hay fever or other upper respiratory allergies:

• runny nose
• itchy nose or throat
• sneezing
• itchy, watery eyes

Warnings

Ask a doctor before use if you have

• glaucoma
• a breathing problem such as emphysema or chronic bronchitis
• trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product

• you may get drowsy
• avoid alcoholic drinks
• alcohol, sedatives & tranquilizers may increase drowsiness
• be careful when driving a motor vehicle or operating machinery
• excitability may occur, especially in children

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.

Directions

• take every 4-6 hours
• do not take more than 6 doses in 24 hours

• adults and children 12 years and over:

  2 teaspoons

• children 6 to under 12 years:

  1 teaspoon

• children under 6 years:

  do not use

Inactive ingredients

Alcohol 5% w/v, benzaldehyde, cherry flavor, FD&C green #3, FD&C yellow #6, glycerin, menthol, methylparaben, propylene glycol, propylparaben, purified water, sucrose, vanillin

Citric acid may be used to adjust pH.

Questions or comments?

call 1-800-645-2158, 9 am - 5 pm ET, Monday - Friday

Other information

Store at room temperature 15°-30°C (59°-86°F).

Avoid freezing. If color fades, potency is not affected.

Rev. 585:02 10/08

Package/Label Principal Display Panel

COMPARE TO ACTIVE INGREDIENT IN CHLOR-TRIMETON®*

Rugby®

NDC: 0536-0370-97

Aller-chlor®

(Chlorpheniramine Maleate Syrup, USP)

ANTIHISTAMINE

Contains Alcohol 5%

*Rugby laboratories, Inc. is not affiliated with the owner of the trademark Chlor-trimeton®. Aller-chlor® is distributed by Rugby Laboratories, Inc.

4 fl oz (118 mL)

Rugby

SATISFACTION GUARANTEED OR YOUR MONEY BACK

Rugby®

Duluth, Georgia 30097

ALLER-CHLOR 
chlorpheniramine maleate syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0536-0370
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BENZALDEHYDE (UNII: TA269SD04T)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)
VANILLIN (UNII: CHI530446X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Product Characteristics
Color	BLUE (blue/green colored) , GREEN (blue/green colored)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0536-0370-97	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2003	07/29/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/17/2003	07/29/2018

Labeler - Rugby Laboratories, Inc. (079246066)

Revised: 12/2019

Document Id: 8461a7c2-5b46-42da-ad0c-5f7991b69d46

34390-5

Set id: 3065bc51-c210-483b-876d-14a4d060bdec

Version: 2

Effective Time: 20191217