childrens pain and fever
Generic: acetaminophen
Labeler: marc glassman, inc.Drug Facts
Product Profile
Brand Name
childrens pain and fever
Generic Name
acetaminophen
Labeler
marc glassman, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68998-525
Product ID
68998-525_46533785-5b8c-8897-e063-6394a90a8075
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2014-10-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68998525
Hyphenated Format
68998-525
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
childrens 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
- 118 mL in 1 BOTTLE (68998-525-24)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46533785-5b8c-8897-e063-6394a90a8075", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["f708e1ec-cf2a-4e2b-851f-f6b703f359b2"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (68998-525-24)", "package_ndc": "68998-525-24", "marketing_start_date": "20141010"}], "brand_name": "Childrens Pain and Fever", "product_id": "68998-525_46533785-5b8c-8897-e063-6394a90a8075", "dosage_form": "LIQUID", "product_ndc": "68998-525", "generic_name": "ACETAMINOPHEN", "labeler_name": "Marc Glassman, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Pain and Fever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141010", "listing_expiration_date": "20261231"}