aquanaz
Generic: dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride
Labeler: capital pharmaceutical, llcDrug Facts
Product Profile
Brand Name
aquanaz
Generic Name
dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride
Labeler
capital pharmaceutical, llc
Dosage Form
TABLET
Routes
Active Ingredients
dextromethorphan hydrobromide 15 mg/1, guaifenesin 400 mg/1, phenylephrine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
29978-587
Product ID
29978-587_4485648d-222a-31b7-e063-6394a90a84e8
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2015-03-10
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
29978587
Hyphenated Format
29978-587
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
aquanaz (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin and phenylephrine hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/1
- 400 mg/1
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (29978-587-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4485648d-222a-31b7-e063-6394a90a84e8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0729978587015"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1552200"], "spl_set_id": ["5e9e4dfd-4def-4756-9bba-d25068640101"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Capital Pharmaceutical, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29978-587-01)", "package_ndc": "29978-587-01", "marketing_start_date": "20150310"}], "brand_name": "Aquanaz", "product_id": "29978-587_4485648d-222a-31b7-e063-6394a90a84e8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "29978-587", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin and Phenylephrine Hydrochloride", "labeler_name": "Capital Pharmaceutical, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aquanaz", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20150310", "listing_expiration_date": "20261231"}