max relief junior

Generic: acetaminophen

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name max relief junior
Generic Name acetaminophen
Labeler atlantic biologicals corp.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0025
Product ID 17856-0025_fde59044-0b07-4f7d-bc67-df823aad1a17
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2023-05-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560025
Hyphenated Format 17856-0025

Supplemental Identifiers

RxCUI
307675
UNII
362O9ITL9D

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 max relief junior (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
source: ndc
Packaging
  • 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-1) / 20.31 mL in 1 CUP, UNIT-DOSE (17856-0025-5)
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-2) / 5 mL in 1 CUP, UNIT-DOSE (17856-0025-6)
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-3) / 15 mL in 1 CUP, UNIT-DOSE (17856-0025-7)
  • 48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0025-4) / 5 mL in 1 SYRINGE (17856-0025-8)
source: ndc

Packages (4)

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fde59044-0b07-4f7d-bc67-df823aad1a17", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307675"], "spl_set_id": ["44730cbd-5b98-49bd-b3b8-6fecb0ccd153"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-1)  / 20.31 mL in 1 CUP, UNIT-DOSE (17856-0025-5)", "package_ndc": "17856-0025-1", "marketing_start_date": "20240228"}, {"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-2)  / 5 mL in 1 CUP, UNIT-DOSE (17856-0025-6)", "package_ndc": "17856-0025-2", "marketing_start_date": "20240228"}, {"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0025-3)  / 15 mL in 1 CUP, UNIT-DOSE (17856-0025-7)", "package_ndc": "17856-0025-3", "marketing_start_date": "20240228"}, {"sample": false, "description": "48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0025-4)  / 5 mL in 1 SYRINGE (17856-0025-8)", "package_ndc": "17856-0025-4", "marketing_start_date": "20240228"}], "brand_name": "MAX relief junior", "product_id": "17856-0025_fde59044-0b07-4f7d-bc67-df823aad1a17", "dosage_form": "LIQUID", "product_ndc": "17856-0025", "generic_name": "Acetaminophen", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAX relief junior", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230514", "listing_expiration_date": "20261231"}