Anti Itch

Product NDC: 67234-008
11-digit product format: 672340008
Labeler code: 67234
Product ID: 67234-008_eba79205-9b9e-495e-a57c-c1d980a90e22
Type: HUMAN OTC DRUG
Nonproprietary name: Pramoxine Hydrochloride and Menthol
Dosage form: CREAM
Route: TOPICAL
Labeler: Natureplex LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2008-01-02
Substance: PRAMOXINE HYDROCHLORIDE; MENTHOL, UNSPECIFIED FORM
Active strength: 10; 10 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product	67234-008		U	Excluded because listing certification expired		excluded / ndc_excluded.zip	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	67234-008	67234-008-01	U	Excluded because listing certification expired		excluded / ndc_excluded.zip	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Anti Itch
Brand name suffix: Maximum Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PRAMOXINE HYDROCHLORIDE	10 mg/g
MENTHOL, UNSPECIFIED FORM	10 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
88AYB867L5	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1116155	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
75de3d5e-ecbe-4d04-a39d-792200e6ee32	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8	Product name	1	20140508
a7051cba-790b-a699-81f8-dbbbdbd9b5ac	Product name	1	20140508
da108d9e-edc8-17a3-8c28-3251c6a8accc	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67234-008-01	Anti Itch Maximum Relief	42 g in 1 TUBE	CREAM	42		4
67234-008-01	Anti Itch Maximum Relief	1 in 1 BOX	CREAM	1		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
Pramoxine Hydrochloride	ACTIVE INGREDIENT	88AYB867L5	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
Menthol	ACTIVE MOIETY	L7T10EIP3A	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
Pramoxine	ACTIVE MOIETY	068X84E056	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)	INACTIVE INGREDIENT	4Q93RCW27E	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
CETOSTEARYL ALCOHOL	INACTIVE INGREDIENT	2DMT128M1S	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
DMDM HYDANTOIN	INACTIVE INGREDIENT	BYR0546TOW	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
POLYSORBATE 60	INACTIVE INGREDIENT	CAL22UVI4M	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67234-008	ANTI ITCH MAXIMUM RELIEF (PRAMOXINE HYDROCHLORIDE AND MENTHOL) CREAM [NATUREPLEX LLC]	3	Current NDC, Legacy NDC, 2 package rows	20250119_75de3d5e-ecbe-4d04-a39d-792200e6ee32.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 102 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
FORTHiQ Pain Relief Lidocaine Patch	PAIN RELIEF LIDOCAINE PATCH	Henan Enokon Medical Instrument Co., Ltd.	2c593420-5788-3422-e063-6394a90a1890	2025-01-22	Warnings	Exact identifier application number: M017
RETALIEF LIDOCAINE 5	LIDOCAINE	Reliable 1 Laboratories LLC	2c262f3c-8cb2-4384-e063-6294a90a436d	2025-01-20	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Roll On Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	1c3e5068-dd61-ebdb-e063-6294a90a97cc	2025-01-20	Warnings	Exact identifier application number: M017
PROHEAL BURN	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	bbc0a5d6-1de6-4ca3-9bb4-a45662b5eab1	2025-01-19	Warnings	Exact identifier application number: M017
HERSTAT PLUS Cold Sore Treatment	CAMPHOR, MENTHOL	Herstat (USA) Inc.	e20ea714-663d-c4ac-e053-2a95a90a5ecc	2025-01-18	Warnings	Exact identifier application number: M017
Pain Relief Medicated	CAMPHOR MENTHOL METHYL SALICYTATE	RITE AID CORPORATION	60895211-69f3-478b-a33f-1c2071f62950	2025-01-16	Warnings	Exact identifier application number: M017
Elgin Pain Relief	MENTHOL	Eco-Logics, Inc.	70eda21e-e566-42f4-9a49-b0d3ad000652	2025-01-16	Warnings	Exact identifier application number: M017
Curist Lidocaine Patch Maximum Strength	LIDOCAINE	Little Pharma, Inc.	e574c188-cc65-287d-e053-2995a90a5972	2025-01-16	Warnings	Exact identifier application number: M017
Equate Hydrocortisone Topical	HYDROCORTISONE	WalMart	1f64555d-f77e-4a83-b222-fdb3ed7d8853	2025-01-16	Warnings	Exact identifier application number: M017
Equate Hydrocortisone	HYDROCORTISONE	WalMart	f5c32b4a-1159-4b7a-b8ac-256d53020dc2	2025-01-16	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Gel-Patch	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	296fcc36-563f-19ca-e063-6394a90ab3ae	2025-01-15	Warnings	Exact identifier application number: M017
K19 RELIEF	MENTHOL	K19 LLC	e2e1ca96-1ae8-4c99-b8de-ce26754292f9	2025-01-15	Warnings	Exact identifier application number: M017
Anecream	LIDOCAINE 4%	Focus Health Group	2d7706e2-7363-4047-96cb-85b718277e8c	2025-01-15	Warnings	Exact identifier application number: M017
Boroleum	CAMPHOR, MENTHOL, WHITE PETROLATUM	Reliable 1 Laboratories	846568af-0fdd-a80e-e053-2a91aa0a9c9e	2025-01-15	Warnings	Exact identifier application number: M017
LidoPro Pain Relief	CAPSAICIN AND LIDOCAINE	Advanced Rx of Tennessee, LLC	27d5997b-1cc2-41c2-e063-6394a90ac74a	2025-01-15	Warnings	Exact identifier application number: M017
Pain Relief Patch 4% Lidocaine	LIDOCAINE	Reliable 1 Laboratories LLC	2b624763-c310-63d9-e063-6394a90a1928	2025-01-15	Warnings	Exact identifier application number: M017
Cannarelief 1000mg	MENTHOL	Carolina Cannabis Creations LLC	01e2ae1a-c969-6dd2-e063-6394a90a9d9e	2025-01-15	Warnings	Exact identifier application number: M017
Healing Hand Cream 2000mg	MENTHOL	Carolina Cannabis Creations LLC	01f8795b-9f95-c793-e063-6394a90a8330	2025-01-15	Warnings	Exact identifier application number: M017
CBD Clinic Deep-Rub Pain Relief - Level 5	CAMPHOR, MENTHOL	ABACUS HEALTH PRODUCTS, INC.	31e2e5cd-d33e-f058-e063-6394a90af7d2	2025-01-14	Warnings	Exact identifier application number: M017
Meijer Odor Free Analgesic Pain Relieving Topical Analgesic	LIDOCAINE HYDROCHLORIDE	Meijer Distribution, Inc	6288efea-f636-4eea-bb9f-78aa2f9af54a	2025-01-14	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
88AYB867L5	PRAMOXINE HYDROCHLORIDE	637-58-1	PRAMOXINE HYDROCHLORIDE
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1116155	menthol 1 % / pramoxine HCl 1 % Topical Cream	PSN	75de3d5e-ecbe-4d04-a39d-792200e6ee32	4
1116155	menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream	SCD	75de3d5e-ecbe-4d04-a39d-792200e6ee32	4
1116155	menthol 1 % / pramoxine hydrochloride 1 % Topical Cream	SY	75de3d5e-ecbe-4d04-a39d-792200e6ee32	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67234-008-01	67234000801	1 TUBE in 1 BOX (67234-008-01) / 42 g in 1 TUBE	1 tube	2008-01-02	0000-00-00	No	No	Current