tanac oral pain reliever

Generic: benzocaine

Labeler: leosons overseas corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tanac oral pain reliever
Generic Name benzocaine
Labeler leosons overseas corp
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

benzocaine 10 g/100mL

Manufacturer
Leosons Overseas Corp

Identifiers & Regulatory

Product NDC 69626-0049
Product ID 69626-0049_26f71ff3-08b2-6177-e063-6394a90ace74
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2015-01-01

Pharmacologic Class

Established (EPC)
standardized chemical allergen [epc]
Chemical Structure
allergens [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 696260049
Hyphenated Format 69626-0049

Supplemental Identifiers

RxCUI
583152 1053339
UNII
U3RSY48JW5
NUI
N0000185508 N0000175629 N0000184306 M0000728

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 tanac oral pain reliever (source: ndc)
Generic Name benzocaine (source: ndc)
Application Number M022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (69626-0049-4) / 13.3 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

benzocaine (10 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "26f71ff3-08b2-6177-e063-6394a90ace74", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["U3RSY48JW5"], "rxcui": ["583152", "1053339"], "spl_set_id": ["81cc61fa-31a7-2214-e053-2a91aa0ae46a"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Leosons Overseas Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69626-0049-4)  / 13.3 mL in 1 BOTTLE", "package_ndc": "69626-0049-4", "marketing_start_date": "20150101"}], "brand_name": "TANAC Oral Pain Reliever", "product_id": "69626-0049_26f71ff3-08b2-6177-e063-6394a90ace74", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "69626-0049", "generic_name": "Benzocaine", "labeler_name": "Leosons Overseas Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TANAC Oral Pain Reliever", "active_ingredients": [{"name": "BENZOCAINE", "strength": "10 g/100mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150101", "listing_expiration_date": "20261231"}