Guaifenesin USP Powder

Pharmaceutical-grade guaifenesin powder meeting USP standards, used as an expectorant in cough syrup formulations. This aromatic ether-alcohol falls under HTS 2909.49.0500 as a chemically defined separate organic compound. It is supplied in bulk for pharmaceutical manufacturing.

Import Duty Rates by Country of Origin

Origin CountryMFN RateCh.99 SurchargesTotal Effective Rate
šŸ‡ØšŸ‡³ChinaFree+35.0%35%
šŸ‡²šŸ‡½MexicoFree+10.0%10%
šŸ‡ØšŸ‡¦CanadaFree+10.0%10%
šŸ‡©šŸ‡ŖGermanyFree+10.0%10%
šŸ‡ÆšŸ‡µJapanFree+10.0%10%

Alternative Classifications

This product could be classified differently depending on its characteristics or intended use.

3004.90Lower: 10% vs 35%

If formulated into tablets or capsules

Finished guaifenesin tablets classify as medicaments in Chapter 30, not as separate chemical compounds.

3824.99Lower: 15% vs 35%

If mixed with excipients as oral solution concentrate

Chemical preparations containing guaifenesin with additives exceed pure compound scope of Chapter 29.

2932.99Lower: 13.7% vs 35%

If containing heterocyclic ring structure misidentified

Only acyclic aromatic ether-alcohols belong in 2909; heterocyclic derivatives move to Chapter 2932.

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Import Tips & Compliance

• Provide Certificate of Analysis (CoA) and USP compliance documentation to verify purity >99%

• Ensure FDA Drug Master File (DMF) registration for active pharmaceutical ingredient importation

• Avoid misclassification as finished dosage form; bulk powder must not be tableted or encapsulated