up and up daytime childrens multi symptom cold
Generic: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler: target corporationDrug Facts
Product Profile
Brand Name
up and up daytime childrens multi symptom cold
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler
target corporation
Dosage Form
SUSPENSION
Routes
Active Ingredients
dextromethorphan hydrobromide 5 mg/5mL, guaifenesin 100 mg/5mL, phenylephrine hydrochloride 2.5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
82442-694
Product ID
82442-694_42d7a5e8-c8bb-0e3f-e063-6294a90a7c4c
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-07-19
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82442694
Hyphenated Format
82442-694
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
up and up daytime childrens multi symptom cold (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
- 100 mg/5mL
- 2.5 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (82442-694-04) / 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": "42d7a5e8-c8bb-0e3f-e063-6294a90a7c4c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "spl_set_id": ["a2d99bc8-7295-4922-acff-0cb02c91273c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (82442-694-04) / 118 mL in 1 BOTTLE", "package_ndc": "82442-694-04", "marketing_start_date": "20240719"}], "brand_name": "UP and UP Daytime Childrens Multi Symptom Cold", "product_id": "82442-694_42d7a5e8-c8bb-0e3f-e063-6294a90a7c4c", "dosage_form": "SUSPENSION", "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": "82442-694", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UP and UP Daytime Childrens Multi Symptom Cold", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "5 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240719", "listing_expiration_date": "20261231"}