GERI-TUSSIN EXPECTORANT- guaifenesin liquid

GERI-TUSSIN EXPECTORANT by

Drug Labeling and Warnings

GERI-TUSSIN EXPECTORANT by is a Otc medication manufactured, distributed, or labeled by Atlantic Biologicals Corps. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (per teaspoonful = 5mL)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings

Do not use if you are hypersensitive to any of the ingredients

Ask a doctor before use if you have

• cough that occurs with too much phlegm (mucus)
• cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor ifcough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

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

• do not take more than 6 doses in any 24-hour period
• do not exceed recommended dose

• adults and children 12 years and over: 2-4 teaspoonfuls every 4 hours
• children under 12 years: ask a doctor

Other information

store at room temperature 15º - 30ºC (59º - 86ºF)

protect from freezing

protect from light

TAMPER EVIDENT: DO NOT USE THIS PRODUCT IF BREAKAWAY BAND ON CAP IS BROKEN OR MISSING

Inactive ingredients

citric acid, caramel, FD and C Red 40, flavor, glycerin, menthol, sodium saccharin, sodium benzoate, sorbitol, water

HOW SUPPLIED

Product: 17856-0793

NDC: 17856-0793-1 15 mL in a CUP, UNIT-DOSE

NDC: 17856-0793-2 10 mL in a CUP, UNIT-DOSE

NDC: 17856-0793-3 5 mL in a CUP, UNIT-DOSE

GERI-TUSSIN EXPECTORANT (GUAIFENESIN) LIQUID

NDC: 17856-0793-1

NDC: 17856-0793-2

NDC: 17856-0793-03

INGREDIENTS AND APPEARANCE

GERI-TUSSIN EXPECTORANT 
guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17856-0793(NDC:57896-793)
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
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARAMEL (UNII: T9D99G2B1R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17856-0793-1	15 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product	05/02/2018
2	NDC: 17856-0793-2	10 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product	05/02/2018
3	NDC: 17856-0793-3	5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product	05/02/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/01/2000

Labeler - Atlantic Biologicals Corps (047437707)

Establishment
Name	Address	ID/FEI	Business Operations
Atlantic Biologicals Corps		047437707	RELABEL(17856-0793) , REPACK(17856-0793)