benzocaine

Generic: benzocaine

Labeler: bellus medical, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benzocaine
Generic Name benzocaine
Labeler bellus medical, llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

benzocaine 200 mg/mL

Manufacturer
Bellus Medical, LLC

Identifiers & Regulatory

Product NDC 71888-101
Product ID 71888-101_47fac2e8-50dd-cddf-e063-6394a90a9176
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2017-06-01

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 71888101
Hyphenated Format 71888-101

Supplemental Identifiers

RxCUI
452688
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 benzocaine (source: ndc)
Generic Name benzocaine (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 12 PACKET in 1 BOX (71888-101-02) / 4 mL in 1 PACKET (71888-101-01)
source: ndc

Packages (1)

Ingredients (1)

benzocaine (200 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47fac2e8-50dd-cddf-e063-6394a90a9176", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["U3RSY48JW5"], "rxcui": ["452688"], "spl_set_id": ["60cafbaf-8ec6-46a5-e053-2a91aa0af11f"], "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": ["Bellus Medical, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 PACKET in 1 BOX (71888-101-02)  / 4 mL in 1 PACKET (71888-101-01)", "package_ndc": "71888-101-02", "marketing_start_date": "20170601"}], "brand_name": "Benzocaine", "product_id": "71888-101_47fac2e8-50dd-cddf-e063-6394a90a9176", "dosage_form": "GEL", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "71888-101", "generic_name": "Benzocaine", "labeler_name": "Bellus Medical, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benzocaine", "active_ingredients": [{"name": "BENZOCAINE", "strength": "200 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170601", "listing_expiration_date": "20271231"}