TUSSIN GUIFENESIN EXPECTRORANT SYRUP- guifenesin syrup

Tussin by

Drug Labeling and Warnings

Tussin by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC, Bio-Pharm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (in each 5ml teaspoonful)

Guaifenesin, USP 100 mg

Purpose

Expectorant

INDICATIONS & USAGE

Helps loosen phlegn (mucus) to make coughs more productive.

WARNINGS

ASK DOCTOR

Ask a doctor before use if

• you have chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
• cough occurs with too much mach phlegm (mucus)

ASK DOCTOR/PHARMACIST

STOP USE

Stop use and ask a doctor if cough lasts for more than 1 week, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a seriuos conditions.

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

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.

PRINCIPAL DISPLAY PANEL

DOSAGE & ADMINISTRATION

INACTIVE INGREDIENT

INGREDIENTS AND APPEARANCE

TUSSIN  GUIFENESIN EXPECTRORANT SYRUP
guifenesin syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61841-403
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CORN SYRUP (UNII: 9G5L16BK6N)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	pink	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61841-403-26	1 in 1 CARTON	01/14/2015
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Export only		01/14/2015

Labeler - Bayer HealthCare LLC (785159372)

Establishment
Name	Address	ID/FEI	Business Operations
Bio-Pharm, Inc.		801652546	manufacture(61841-403) , pack(61841-403)