myderm bite relief

Generic: benzocaine

Labeler: inspec solutions llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name myderm bite relief
Generic Name benzocaine
Labeler inspec solutions llc.
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

benzocaine 5 g/100g

Manufacturer
Inspec Solutions LLC.

Identifiers & Regulatory

Product NDC 72667-019
Product ID 72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2021-12-14

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 72667019
Hyphenated Format 72667-019

Supplemental Identifiers

RxCUI
251295
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 myderm bite relief (source: ndc)
Generic Name benzocaine (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 g/100g
source: ndc
Packaging
  • 50 g in 1 TUBE (72667-019-01)
source: ndc

Packages (1)

Ingredients (1)

benzocaine (5 g/100g)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2d07a8c9-17a4-1727-e063-6394a90a801d", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["U3RSY48JW5"], "rxcui": ["251295"], "spl_set_id": ["88615668-16b5-7840-e053-2a95a90a9208"], "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": ["Inspec Solutions LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (72667-019-01)", "package_ndc": "72667-019-01", "marketing_start_date": "20211214"}], "brand_name": "MyDerm Bite Relief", "product_id": "72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d", "dosage_form": "OINTMENT", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "72667-019", "generic_name": "Benzocaine", "labeler_name": "Inspec Solutions LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MyDerm Bite Relief", "active_ingredients": [{"name": "BENZOCAINE", "strength": "5 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}