Air Power
Air Power is an FDA drug label for the active ingredient GUAIFENESIN manufactured by Schwabe North America, Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260527.
- Generic name
- GUAIFENESIN
- Manufacturer
- Schwabe North America, Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 53499-0232
- Application
- M012
- Label effective
- 20260527
About this product
Air Power is an FDA-registered drug product whose active ingredient is GUAIFENESIN. It is labelled by Schwabe North America, Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 53499-0232, application M012, label effective 20260527. It is one of 98 FDA drug label records sharing the active ingredient GUAIFENESIN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing GUAIFENESIN are most often described in connection with: indications usage, helps loosen, phlegm mucus, thin bronchial, secretions rid, make coughs. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Indications & Usage: Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.
Dosage & Administration
Dosage & Administration: Adults & children 12 years of age and older: 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 & Usage: Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.
Warnings
Warnings: Do not use this product if you are pregnant, attempting to become pregnant, or breast-feeding.
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View labelHow products containing GUAIFENESIN compare
FDA lists 98 drug label records with GUAIFENESIN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Bryant Ranch Prepack | 4 |
| — | — | Strategic Sourcing Services LLC | 4 |
| — | — | CVS Pharmacy | 3 |
| — | — | Cardinal Health 107, LLC | 3 |
| — | — | Reckitt Benckiser LLC | 3 |
Frequently asked questions
What is Air Power used for?
Indications & Usage: Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.
Who makes Air Power?
Schwabe North America, Inc is the labeler of record for Air Power. 98 FDA label records share the active ingredient GUAIFENESIN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Air Power come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Air Power prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing GUAIFENESIN?
Yes. 98 FDA drug label records list GUAIFENESIN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Air Power been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.