mejoralito
Generic: acetaminophen
Labeler: opmx llcDrug Facts
Product Profile
Brand Name
mejoralito
Generic Name
acetaminophen
Labeler
opmx llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
acetaminophen 160 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
69729-068
Product ID
69729-068_3d82e9f0-27d7-054f-e063-6294a90ab575
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2021-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69729068
Hyphenated Format
69729-068
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
mejoralito (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/5mL
Packaging
- 60 mL in 1 BOTTLE (69729-068-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d82e9f0-27d7-054f-e063-6294a90ab575", "openfda": {"upc": ["0810053180259", "0860006095161"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["5b8a92c9-47c0-4438-a49d-b3878f7afd73"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (69729-068-02)", "package_ndc": "69729-068-02", "marketing_start_date": "20210201"}], "brand_name": "Mejoralito", "product_id": "69729-068_3d82e9f0-27d7-054f-e063-6294a90ab575", "dosage_form": "SUSPENSION", "product_ndc": "69729-068", "generic_name": "Acetaminophen", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mejoralito", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}