Do Me Delay Cream

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 Cream
Generic name: BENZOCAINE
Manufacturer: Prodigy Media
Product type: HUMAN OTC DRUG
SPL set ID: 53d5cd6b-96b8-9ba2-e063-6294a90a0d15
SPL ID: 53d5cd6b-96b9-9ba2-e063-6294a90a0d15
Version: 1
Effective date: 2026-07-24
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:43

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 Cream	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Prodigy Media	openfda.manufacturer_name
ndc	package	70171-0052-1	openfda.package_ndc
ndc	product	70171-0052	openfda.product_ndc
ndc11	package	70171005201	derived:openfda.package_ndc
spl id		53d5cd6b-96b9-9ba2-e063-6294a90a0d15	id
spl set id		53d5cd6b-96b8-9ba2-e063-6294a90a0d15	set_id
unii		U3RSY48JW5	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 Premature ejaculation may be due to a condition requiring medical supervision. If this product used as directed, does not provide relief, discontinue use and consult a doctor. Stop use and ask a doctor if If you or your partner develops a rash or irritation, such as burning or itching, discontinue use. If symptoms persist consult a doctor. Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away..

Reported adverse events (FAERS/openFDA)#

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