childrens acetaminophen
Generic: acetaminophen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
childrens acetaminophen
Generic Name
acetaminophen
Labeler
proficient rx lp
Dosage Form
SUSPENSION
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
71205-406
Product ID
71205-406_05ce8796-5e1b-4ff7-8d77-b4bf55ea7625
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2014-04-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205406
Hyphenated Format
71205-406
Supplemental Identifiers
RxCUI
UPC
UNII
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 acetaminophen (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 (71205-406-04) / 118 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": "05ce8796-5e1b-4ff7-8d77-b4bf55ea7625", "openfda": {"upc": ["0371205406042"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["35ec3a0e-0776-4d04-935f-96ad4fbb6d3a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71205-406-04) / 118 mL in 1 BOTTLE", "package_ndc": "71205-406-04", "marketing_start_date": "20200219"}], "brand_name": "childrens acetaminophen", "product_id": "71205-406_05ce8796-5e1b-4ff7-8d77-b4bf55ea7625", "dosage_form": "SUSPENSION", "product_ndc": "71205-406", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "childrens acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140409", "listing_expiration_date": "20261231"}