up and up powderlax
Generic: polyethylene glycol 3350
Labeler: target corporationDrug Facts
Product Profile
Brand Name
up and up powderlax
Generic Name
polyethylene glycol 3350
Labeler
target corporation
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
polyethylene glycol 3350 17 g/17g
Manufacturer
Identifiers & Regulatory
Product NDC
11673-306
Product ID
11673-306_cf711078-27fb-4e55-8f5a-7aaab810b483
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA090685
Listing Expiration
2026-12-31
Marketing Start
2009-10-07
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673306
Hyphenated Format
11673-306
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
up and up powderlax (source: ndc)
Generic Name
polyethylene glycol 3350 (source: ndc)
Application Number
ANDA090685 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 17 g/17g
Packaging
- 119 g in 1 BOTTLE (11673-306-01)
- 238 g in 1 BOTTLE (11673-306-02)
- 510 g in 1 BOTTLE (11673-306-03)
- 765 g in 1 BOTTLE (11673-306-09)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf711078-27fb-4e55-8f5a-7aaab810b483", "openfda": {"nui": ["N0000010288", "N0000175811", "N0000009871"], "unii": ["G2M7P15E5P"], "rxcui": ["876193"], "spl_set_id": ["1bceb457-b24f-485d-bfe2-af4b7d38a5c2"], "pharm_class_pe": ["Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Osmotic Laxative [EPC]"], "pharm_class_moa": ["Osmotic Activity [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "119 g in 1 BOTTLE (11673-306-01)", "package_ndc": "11673-306-01", "marketing_start_date": "20190412"}, {"sample": false, "description": "238 g in 1 BOTTLE (11673-306-02)", "package_ndc": "11673-306-02", "marketing_start_date": "20091007"}, {"sample": false, "description": "510 g in 1 BOTTLE (11673-306-03)", "package_ndc": "11673-306-03", "marketing_start_date": "20091007"}, {"sample": false, "description": "765 g in 1 BOTTLE (11673-306-09)", "package_ndc": "11673-306-09", "marketing_start_date": "20161021"}], "brand_name": "up and up powderlax", "product_id": "11673-306_cf711078-27fb-4e55-8f5a-7aaab810b483", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "11673-306", "generic_name": "Polyethylene Glycol 3350", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up powderlax", "active_ingredients": [{"name": "POLYETHYLENE GLYCOL 3350", "strength": "17 g/17g"}], "application_number": "ANDA090685", "marketing_category": "ANDA", "marketing_start_date": "20091007", "listing_expiration_date": "20261231"}