Anti Itch Maximum Relief

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: Anti Itch Maximum Relief
Generic name: PRAMOXINE HYDROCHLORIDE AND MENTHOL
Manufacturer: Natureplex LLC
Product type: HUMAN OTC DRUG
SPL set ID: 75de3d5e-ecbe-4d04-a39d-792200e6ee32
SPL ID: eba79205-9b9e-495e-a57c-c1d980a90e22
Version: 4
Effective date: 2025-08-28
Source export date: 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:35

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Anti Itch Maximum Relief	openfda.brand_name
generic name		PRAMOXINE HYDROCHLORIDE AND MENTHOL	openfda.generic_name
manufacturer name		Natureplex LLC	openfda.manufacturer_name
ndc	package	67234-008-01	openfda.package_ndc
ndc	product	67234-008	openfda.product_ndc
ndc11	package	67234000801	derived:openfda.package_ndc
rxcui		1116155	openfda.rxcui
spl id		eba79205-9b9e-495e-a57c-c1d980a90e22	id
spl set id		75de3d5e-ecbe-4d04-a39d-792200e6ee32	set_id
unii		L7T10EIP3A	openfda.unii
unii		88AYB867L5	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 and nose. Not for prolonged use. Do not use on large areas of the body 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 redness, irritation, swelling, or pain develops, persists, or increases If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Reported adverse events (FAERS/openFDA)#

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