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 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 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
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?

1-800-426-9391

HOW SUPPLIED

Chlorpheniramine Maleate 4 mg

NDC: 71335-2056-1: 30 Tablets in a BOTTLE, PLASTIC

NDC: 71335-2056-2: 60 Tablets in a BOTTLE, PLASTIC

NDC: 71335-2056-3: 100 Tablets in a BOTTLE, PLASTIC

NDC: 71335-2056-4: 120 Tablets in a BOTTLE, PLASTIC

NDC: 71335-2056-5: 40 Tablets in a BOTTLE, PLASTIC

NDC: 71335-2056-6: 24 Tablets in a BOTTLE, PLASTIC

Repackaged/Relabeled by:

Bryant Ranch Prepack, Inc.
Burbank, CA 91504

Chlorpheniramine Maleate 4 mg Tablet

ALLERGY
chlorpheniramine maleate tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71335-2056(NDC:0904-0012)
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71335-2056-1	30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/02/2022
2	NDC:71335-2056-2	60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2024
3	NDC:71335-2056-3	100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2024
4	NDC:71335-2056-4	120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2024
5	NDC:71335-2056-5	40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2024
6	NDC:71335-2056-6	24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/03/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	12/19/1992

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)

Name	Address	ID/FEI	Business Operations
Establishment
Bryant Ranch Prepack		171714327	REPACK(71335-2056) , RELABEL(71335-2056)

Major 44-194