H2Ocean NOTHING TATTOO GLIDE AFTERCARE MAX STRENGTH

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: H2Ocean NOTHING TATTOO GLIDE AFTERCARE MAX STRENGTH
Generic name: LIDOCAINE HCL
Manufacturer: H2Ocean, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 386bf11b-1d71-44bf-e063-6394a90a2817
SPL ID: 386bf11b-1d72-44bf-e063-6394a90a2817
Version: 1
Effective date: 2025-06-25
Source export date: 2026-10-30
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:11:45

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		H2Ocean NOTHING TATTOO GLIDE AFTERCARE MAX STRENGTH	openfda.brand_name
generic name		LIDOCAINE HCL	openfda.generic_name
manufacturer name		H2Ocean, LLC	openfda.manufacturer_name
ndc	package	70411-200-01	openfda.package_ndc
ndc	package	70411-200-07	openfda.package_ndc
ndc	product	70411-200	openfda.product_ndc
ndc11	package	70411020001	derived:openfda.package_ndc
ndc11	package	70411020007	derived:openfda.package_ndc
rxcui		1858984	openfda.rxcui
spl id		386bf11b-1d72-44bf-e063-6394a90a2817	id
spl set id		386bf11b-1d71-44bf-e063-6394a90a2817	set_id
unii		98PI200987	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. Do not use • in the eyes or apply over large areas of the body • longer than 1 week unless directed by a doctor •in large quantities, particularly over raw surfaces or blistered areas Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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