pain and fever
Generic: acetaminophen
Labeler: kroger companyDrug Facts
Product Profile
Brand Name
pain and fever
Generic Name
acetaminophen
Labeler
kroger company
Dosage Form
SUSPENSION
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
30142-590
Product ID
30142-590_b5d14a88-eca7-4e54-af85-9d77be92c85e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1993-03-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
30142590
Hyphenated Format
30142-590
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
pain and fever (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (30142-590-16) / 59 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5d14a88-eca7-4e54-af85-9d77be92c85e", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["d181560c-1c39-4f2e-8a17-996224ca040f"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-590-16) / 59 mL in 1 BOTTLE", "package_ndc": "30142-590-16", "marketing_start_date": "20120315"}], "brand_name": "pain and fever", "product_id": "30142-590_b5d14a88-eca7-4e54-af85-9d77be92c85e", "dosage_form": "SUSPENSION", "product_ndc": "30142-590", "generic_name": "acetaminophen", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain and fever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19930331", "listing_expiration_date": "20261231"}