acetaminophen
Generic: acetaminophen
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cvs pharmacy
Dosage Form
SOLUTION
Routes
Active Ingredients
acetaminophen 1000 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
69842-445
Product ID
69842-445_281998c3-1b4c-431a-a566-6a05a89a9618
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2021-04-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842445
Hyphenated Format
69842-445
Supplemental Identifiers
RxCUI
UNII
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
acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/30mL
Packaging
- 237 mL in 1 BOTTLE, PLASTIC (69842-445-19)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "281998c3-1b4c-431a-a566-6a05a89a9618", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["258975d2-d8e8-407d-9804-df3b37a184e4"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (69842-445-19)", "package_ndc": "69842-445-19", "marketing_start_date": "20210409"}], "brand_name": "Acetaminophen", "product_id": "69842-445_281998c3-1b4c-431a-a566-6a05a89a9618", "dosage_form": "SOLUTION", "product_ndc": "69842-445", "generic_name": "Acetaminophen", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210409", "listing_expiration_date": "20261231"}