AIR POWER- guaifenesin tablet

Air Power by

Drug Labeling and Warnings

Air Power by is a Otc medication manufactured, distributed, or labeled by Schwabe North America, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient:

Guaifenesin 200 mg

Inactive Ingredients:

Carnauba Wax

Cellulose

Fenugreek (seed) Extract

Glycerin

Hypromellose

Magnesium Stearate

Maltodextrin

Marshmallow (root) Extract

Povidone

Silica

Sodium Croscarmellose

Stearic Acid

Dosage & Administration:

Adults & children 12 years and over:  take 1-2 tablets every 4 hours, not to exceed 12 tablets in 24 hours

Children 6 to 11 years of age: take ½ to 1 tablet every 4 hours, not to exceed 6 tablets in 24 hours

Children under 6 years of age: consult a doctor before use

Purpose:

Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.

Indications & Useage:

Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.

Warnings: 

Do not use this product if you are pregnant, attempting to become pregnant, or breast-feeding. 

Ask a doctor:

Ask a doctor before use if you have a persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, a cough that is accompanied by excessive phlegm (mucus), diabetes, been taking any medications. 

Stop Use:

Stop use and ask a doctor if cough persists more than 7 days, tends to recur, or is accompanied by a fever, rash or persisient headache.

A persistent cough may be a sign of a serious condition.

If you are taking any medications, consult a healthcare professional before use. 

Keep out of Reach of Children:

Keep out of the reach of children.

Overdosage:

In case of overdose, seek medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

AIR POWER  
guaifenesin tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53499-0232
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg

Inactive Ingredients
Ingredient Name	Strength
CARNAUBA WAX (UNII: R12CBM0EIZ)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
FENUGREEK SEED (UNII: 654825W09Z)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
POVIDONE (UNII: FZ989GH94E)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	brown (light brown to gray-brown w/ light and/or dark specks)	Score	no score
Shape	OVAL (Convex face, debossed 232 tablet)	Size	20mm
Flavor		Imprint Code	232
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53499-0232-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	06/14/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	06/14/2021

Labeler - Schwabe North America, Inc (831153908)

Establishment
Name	Address	ID/FEI	Business Operations
Schwabe North America, Inc		831153908	manufacture(53499-0232)