pain relief extra strength

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler h e b
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-195
Product ID 37808-195_eef88a02-d62d-47e1-85f1-16d3d20e86d1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2004-05-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808195
Hyphenated Format 37808-195

Supplemental Identifiers

RxCUI
198440
UPC
0041220359882
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 extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 225 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-195-20)
source: ndc

Packages (3)

37808-195-08 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 37808-195-12 1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 37808-195-20 225 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-195-20)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eef88a02-d62d-47e1-85f1-16d3d20e86d1", "openfda": {"upc": ["0041220359882"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["99699cd6-ba7d-4db0-9f0f-0f2c1a369138"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-195-08)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-195-08", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-195-12)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "37808-195-12", "marketing_start_date": "20040510"}, {"sample": false, "description": "225 TABLET, COATED in 1 BOTTLE, PLASTIC (37808-195-20)", "package_ndc": "37808-195-20", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength", "product_id": "37808-195_eef88a02-d62d-47e1-85f1-16d3d20e86d1", "dosage_form": "TABLET, COATED", "product_ndc": "37808-195", "generic_name": "Acetaminophen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040510", "listing_expiration_date": "20271231"}