DO ME DELAY

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: DO ME DELAY
Generic name: LIDOCAINE HCL
Manufacturer: Prodigy Media Inc
Product type: HUMAN OTC DRUG
SPL set ID: 5255ee85-6f29-0776-e063-6394a90a525b
SPL ID: 5255ee85-6f2a-0776-e063-6394a90a525b
Version: 1
Effective date: 2026-05-21
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:42

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		DO ME DELAY	openfda.brand_name
generic name		LIDOCAINE HCL	openfda.generic_name
manufacturer name		Prodigy Media Inc	openfda.manufacturer_name
ndc	package	70171-0051-1	openfda.package_ndc
ndc	product	70171-0051	openfda.product_ndc
ndc11	package	70171005101	derived:openfda.package_ndc
spl id		5255ee85-6f2a-0776-e063-6394a90a525b	id
spl set id		5255ee85-6f29-0776-e063-6394a90a525b	set_id
unii		V13007Z41A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings . For external use only. . Avoid contact with eyes Stop use and ask a doctor if . Condition worsens or symptoms persist for more than 7 days . Symploms clear up and occur again within a few days . Do not use in large quantities, particulary over raw surfaces or blistered areas. Do not exceed the recommended daily dosage unless directed by a doctor. Do not use . On wounds or damaged skin.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.