pain relief

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name 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 37808-130
Product ID 37808-130_2b505669-63d4-4277-8cf6-bfb24a221592
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1996-04-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808130
Hyphenated Format 37808-130

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 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 in 1 CARTON (37808-130-26) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

37808-130-26 1 BOTTLE in 1 CARTON (37808-130-26) / 118 mL in 1 BOTTLE

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

pain relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b505669-63d4-4277-8cf6-bfb24a221592", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["3258ef39-c36e-4a97-8631-89b8d4caf058"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-130-26)  / 118 mL in 1 BOTTLE", "package_ndc": "37808-130-26", "marketing_start_date": "19960429"}], "brand_name": "pain relief", "product_id": "37808-130_2b505669-63d4-4277-8cf6-bfb24a221592", "dosage_form": "SUSPENSION", "product_ndc": "37808-130", "generic_name": "Acetaminophen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19960429", "listing_expiration_date": "20261231"}