bactimicina cough and cold
Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler: dlc laboratories, inc.Drug Facts
Product Profile
Brand Name
bactimicina cough and cold
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler
dlc laboratories, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 100 mg/5mL, phenylephrine hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
24286-1546
Product ID
24286-1546_47d53810-ddd7-346c-e063-6394a90a6cd4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2027-12-31
Marketing Start
2013-11-06
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
242861546
Hyphenated Format
24286-1546
Supplemental Identifiers
RxCUI
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
bactimicina cough and cold (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
- 100 mg/5mL
- 5 mg/5mL
Packaging
- 1 BOTTLE in 1 BOX (24286-1546-4) / 118 mL in 1 BOTTLE
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47d53810-ddd7-346c-e063-6394a90a6cd4", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1044949"], "spl_set_id": ["2e612c62-9bbb-45f2-a253-aa2bfaeaac70"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (24286-1546-4) / 118 mL in 1 BOTTLE", "package_ndc": "24286-1546-4", "marketing_start_date": "20131106"}], "brand_name": "BACTIMICINA COUGH AND COLD", "product_id": "24286-1546_47d53810-ddd7-346c-e063-6394a90a6cd4", "dosage_form": "SOLUTION", "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": "24286-1546", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BACTIMICINA COUGH AND COLD", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131106", "listing_expiration_date": "20271231"}