Outgro

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: Outgro
Generic name: BENZOCAINE
Manufacturer: Medtech Products Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d6be8a1d-aca7-42b1-86da-881d42ffe8d5
SPL ID: 43f87627-6147-4dc2-b4cf-1994fbfb1067
Version: 5
Effective date: 2024-10-25
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:37:38

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		Outgro	openfda.brand_name
generic name		BENZOCAINE	openfda.generic_name
manufacturer name		Medtech Products Inc.	openfda.manufacturer_name
ndc	package	63029-531-11	openfda.package_ndc
ndc	product	63029-531	openfda.product_ndc
ndc11	package	63029053111	derived:openfda.package_ndc
spl id		43f87627-6147-4dc2-b4cf-1994fbfb1067	id
spl set id		d6be8a1d-aca7-42b1-86da-881d42ffe8d5	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. ■ Extremely Flammable . Keep away from fire or flame. Avoid smoking during use and until product has dried. When using this product: avoid contact with eyes. Stop use and ask a doctor if: ■ condition worsens ■ condition does not improve in 7 days ■ condition clears up and occurs again within a few days. Keep out of the reach of children. If 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.