iodent oral analgesic

Generic: benzocaine

Labeler: united exchange corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name iodent oral analgesic
Generic Name benzocaine
Labeler united exchange corp.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

benzocaine 200 mg/g

Manufacturer
United Exchange Corp.

Identifiers & Regulatory

Product NDC 65923-094
Product ID 65923-094_4262e1af-6041-bc2d-e063-6294a90a006f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2018-01-02

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 65923094
Hyphenated Format 65923-094

Supplemental Identifiers

RxCUI
238910
UPC
0831527004901
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 iodent oral analgesic (source: ndc)
Generic Name benzocaine (source: ndc)
Application Number M022 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (65923-094-11) / 11.9 g in 1 TUBE
source: ndc

Packages (1)

65923-094-11 1 TUBE in 1 CARTON (65923-094-11) / 11.9 g in 1 TUBE

Ingredients (1)

benzocaine (200 mg/g)

Linked Drug Pages (1)

Iodent Oral Analgesic ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4262e1af-6041-bc2d-e063-6294a90a006f", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["0831527004901"], "unii": ["U3RSY48JW5"], "rxcui": ["238910"], "spl_set_id": ["63902125-f8dc-0ada-e053-2991aa0a7ce5"], "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": ["United Exchange Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (65923-094-11)  / 11.9 g in 1 TUBE", "package_ndc": "65923-094-11", "marketing_start_date": "20180102"}], "brand_name": "Iodent Oral Analgesic", "product_id": "65923-094_4262e1af-6041-bc2d-e063-6294a90a006f", "dosage_form": "GEL", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "65923-094", "generic_name": "Benzocaine", "labeler_name": "United Exchange Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Iodent Oral Analgesic", "active_ingredients": [{"name": "BENZOCAINE", "strength": "200 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180102", "listing_expiration_date": "20261231"}