pain reliever
Generic: acetaminophen
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
pain reliever
Generic Name
acetaminophen
Labeler
rite aid corporation
Dosage Form
SOLUTION
Routes
Active Ingredients
acetaminophen 1000 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
11822-8003
Product ID
11822-8003_97aa0aa5-61e1-4b9a-9800-29be11306cc2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2027-12-31
Marketing Start
2023-05-04
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118228003
Hyphenated Format
11822-8003
Supplemental Identifiers
RxCUI
UPC
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
pain reliever (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 (11822-8003-9)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "97aa0aa5-61e1-4b9a-9800-29be11306cc2", "openfda": {"upc": ["0011822231060"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["9a647967-f0c6-466e-be70-34fd3de0a803"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (11822-8003-9)", "package_ndc": "11822-8003-9", "marketing_start_date": "20230504"}], "brand_name": "Pain Reliever", "product_id": "11822-8003_97aa0aa5-61e1-4b9a-9800-29be11306cc2", "dosage_form": "SOLUTION", "product_ndc": "11822-8003", "generic_name": "Acetaminophen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230504", "listing_expiration_date": "20271231"}