safetussin non drowsy cough plus chest congestion
Generic: dextromethorphan hydrobromide, and guaifenesin
Labeler: kramer laboratoriesDrug Facts
Product Profile
Brand Name
safetussin non drowsy cough plus chest congestion
Generic Name
dextromethorphan hydrobromide, and guaifenesin
Labeler
kramer laboratories
Dosage Form
LIQUID
Routes
Active Ingredients
dextromethorphan hydrobromide 10 mg/5mL, guaifenesin 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
55505-220
Product ID
55505-220_cff65bfa-6667-4ecf-a98c-a93b50d2d161
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2023-06-01
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55505220
Hyphenated Format
55505-220
Supplemental Identifiers
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
safetussin non drowsy cough plus chest congestion (source: ndc)
Generic Name
dextromethorphan hydrobromide, and guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
- 100 mg/5mL
Packaging
- 118 mL in 1 BOTTLE, PLASTIC (55505-220-33)
- 237 mL in 1 BOTTLE, PLASTIC (55505-220-36)
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cff65bfa-6667-4ecf-a98c-a93b50d2d161", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "spl_set_id": ["60311ca3-8544-417e-aa29-e9f65c6692ba"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KRAMER LABORATORIES"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (55505-220-33)", "package_ndc": "55505-220-33", "marketing_start_date": "20250701"}, {"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (55505-220-36)", "package_ndc": "55505-220-36", "marketing_start_date": "20230601"}], "brand_name": "SAFETUSSIN Non Drowsy Cough plus chest congestion", "product_id": "55505-220_cff65bfa-6667-4ecf-a98c-a93b50d2d161", "dosage_form": "LIQUID", "pharm_class": ["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]"], "product_ndc": "55505-220", "generic_name": "Dextromethorphan Hydrobromide, and Guaifenesin", "labeler_name": "KRAMER LABORATORIES", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SAFETUSSIN Non Drowsy", "brand_name_suffix": "Cough plus chest congestion", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}