childrens pain relief

Generic: acetaminophen

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name childrens pain relief
Generic Name acetaminophen
Labeler h e b
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-482
Product ID 37808-482_b4de4354-f780-4447-b679-19bc4a5c067f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2015-03-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808482
Hyphenated Format 37808-482

Supplemental Identifiers

RxCUI
307668
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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 relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (37808-482-04) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

37808-482-04 1 BOTTLE, PLASTIC in 1 BOX (37808-482-04) / 118 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

Childrens Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4de4354-f780-4447-b679-19bc4a5c067f", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["a0c0277e-50aa-4328-8f93-ab20c6176b2b"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-482-04)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "37808-482-04", "marketing_start_date": "20150308"}], "brand_name": "Childrens Pain Relief", "product_id": "37808-482_b4de4354-f780-4447-b679-19bc4a5c067f", "dosage_form": "SUSPENSION", "product_ndc": "37808-482", "generic_name": "Acetaminophen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150308", "listing_expiration_date": "20261231"}