ALLERGY- chlorpheniramine maleate tablet

Allergy by

Drug Labeling and Warnings

Allergy by is a Otc medication manufactured, distributed, or labeled by Major Pharmaceuticals, LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Chlorpheniramine maleate 4 mg

Purpose

Antihistamine

Uses

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

• runny nose
• itchy, watery eyes
• sneezing
• itching of the nose or throat

Warnings

Do not use

to make a child sleepy.

Ask a doctor before use if you have

• a breathing problem such as emphysema or chronic bronchitis  
• glaucoma
• difficulty in urination due to enlargement of the prostate gland
  

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

• drowsiness may occur
• avoid alcoholic beverages
• alcohol, sedatives, and tranquilizers may increase drowsiness
• use caution 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 (1-800-222-1222) right away.

Directions

• take every 4 to 6 hours, or as directed by a doctor
  

• adults and children 12 years and over: 1 tablet. Do not exceed 6 tablets ; in 24 hours.
• children 6 to under 12 years: 1/2 tablet (break tablet in half). ; Do not exceed 3 whole tablets in ; 24 hours.
• children under 6 years: do not use

Other information

• TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
  
• store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
• protect from excessive moisture
• see end flap for expiration date and lot number

Inactive ingredients

corn starch, D&C yellow #10 aluminum lake, lactose anhydrous, magnesium stearate, microcrystalline cellulose

Questions or comments?

(800) 616-2471

Principal Display Panel

MAJOR®

NDC: 0904-0012-24

4 Hour

Allergy Tablets
Chlorpheniramine Maleate
4 mg
Antihistamine

Relieves:
Sneezing, Runny Nose,
Itchy, Watery Eyes,
Itchy Throat

Actual Size

24 Tablets

TAMPER EVIDENT: DO NOT USE IF PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
50844              REV0419ML19412

Distributed by:
MAJOR® PHARMACEUTICALS
17177 N Laurel Park Drive, Suite 233
Livonia, MI 48152
Rev. 10/19         M-17       Re-order No. 700790

Major 44-194

Principal Display Panel - Unit Dose

NDC: 0904-0012-61

MAJOR®

Unit Dose

ALLERGY TABLETS
CHLORPHENIRAMINE MALEATE

Antihistamine

4 mg
100 TABLETS

This Unit Dose package is not child resistant and is Intended for Institutional Use Only.

50844     REV0419B19412

Distributed by:
MAJOR® PHARMACEUTICALS
17177 N Laurel Park Drive, Suite 233
Livonia, MI 48152

Rev. 10/19    M-17  Re-order   No. 301560

Major 44-194-DSP

INGREDIENTS AND APPEARANCE

ALLERGY 
chlorpheniramine maleate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0904-0012
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	4 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	YELLOW	Score	2 pieces
Shape	ROUND	Size	8mm
Flavor		Imprint Code	44;194
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0904-0012-61	10 in 1 CARTON	12/19/1992
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 0904-0012-24	2 in 1 CARTON	12/19/1992
2		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC: 0904-0012-59	1 in 1 CARTON	12/19/1992
3		100 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 0904-0012-80	1000 in 1 BOTTLE; Type 0: Not a Combination Product	12/19/1992

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	12/19/1992

Labeler - Major Pharmaceuticals (191427277)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867894	MANUFACTURE(0904-0012)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		038154464	PACK(0904-0012)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		967626305	PACK(0904-0012)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		832867837	PACK(0904-0012)

Establishment
Name	Address	ID/FEI	Business Operations
LNK International, Inc.		868734088	PACK(0904-0012)