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 110 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dollar General Cold-Hot Medicated Patches	MENTHOL	DOLGENCORP, LLC	c6e0388b-af9e-4e51-8f94-6788185c31a0	2024-12-18	Warnings	Exact identifier application number: M017
THERA CARE PAIN THERAPY	LIDOCAINE	Veridian Healthcare	e023bb5a-a4bc-4681-a1f4-48ca0d2cb102	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Medicated Pain Relief Patches	CAMPHOR, MENTHOL, METHYL SALICYLATE	Veridian Healthcare	f6f3c9c0-d6e3-75a3-e053-6294a90a1965	2024-12-18	Warnings	Exact identifier application number: M017
Good Sense Hot and Cold Medicated Patch	MENTHOL	GOOD SENSE	1b16c3e5-a29f-4043-94e6-0a0e0ea3d93e	2024-12-18	Warnings	Exact identifier application number: M017
Hunter Beach 4%	LIDOCAINE	HUNTERS BEACH LIFE	f2ef9c12-6e42-486b-b6f2-0ad534e94294	2024-12-18	Warnings	Exact identifier application number: M017
Hunter Beach 4%	LIDOCAINE	HUNTERS BEACH LIFE	05a9605b-0d01-4333-8e54-7202e7c31c49	2024-12-18	Warnings	Exact identifier application number: M017
Ultra Strength Muscle Rub	CAMPHOR, MENTHOL, METHYL SALICYLATE	The Mentholatum Company	32b64985-0e2f-49ee-9840-946d7279fee7	2024-12-17	Warnings	Exact identifier application number: M017
CVS Health Cold and Hot Pain Relieving Extra Strength	MENTHOL, METHYL SALICYLATE	CVS Pharmacy	1ca1a631-cb2c-46cd-bd41-05469b08d208	2024-12-17	Warnings	Exact identifier application number: M017
Mentholatum Pain Relieving	MENTHOL, METHYL SALICYLATE	The Mentholatum Company	0056b952-9870-485a-9f35-f985472875a9	2024-12-17	Warnings	Exact identifier application number: M017
Mentholatum Lidocaine Heat	LIDOCAINE HCL	The Mentholatum Company	cc2ef25a-b569-4d48-a666-899f710b4b34	2024-12-17	Warnings	Exact identifier application number: M017
Rite Aid Muscle Rub Ultra Strength	CAMPHOR, MENTHOL, METHYL SALICYLATE	Rite Aid Corporation	039fff40-b5ba-42cb-932c-8a70ca92759d	2024-12-17	Warnings	Exact identifier application number: M017
Signature Care Cold and Hot Medicated	MENTHOL	Safeway	88f59f95-0a7c-458c-949c-0dff16ad94e4	2024-12-17	Warnings	Exact identifier application number: M017
Equate Cool and Heat	MENTHOL, METHYL SALICYLATE	Wal-Mart Stores Inc	c5ab2426-eeca-4ba4-9f00-7790d2176471	2024-12-17	Warnings	Exact identifier application number: M017
CVS Health Muscle Rub Ultra Strength	CAMPHOR, MENTHOL, METHYL SALICYLATE	CVS Pharmacy	4fc0d6bb-efa7-40cf-a6d5-e0feaa93c80a	2024-12-17	Warnings	Exact identifier application number: M017
DG Health Maximum Strength Pain Relieving Cleansing	BENZALKONIUM CL, LIDOCAINE HCL	Dollar General Corporation	64f69315-77a3-49dc-940d-efd7a29c6645	2024-12-17	Warnings	Exact identifier application number: M017
Chiggerex	BENZOCAINE	RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH	5e5d84ab-f57f-448d-a4c1-ced38890eec2	2024-12-17	Warnings	Exact identifier application number: M017
DerMend Moisturizing Anti-Itch	PRAMOXINE HYDROCHLORIDE	Ferndale Laboratories, Inc.	14c7fb1c-a310-4b12-ab2e-7f1c0801995c	2024-12-17	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Geri-Care Pharmaceuticals, Corp	fd67566a-1076-019d-e053-6394a90a415c	2024-12-17	Warnings	Exact identifier application number: M017
Extra Strength	MENTHOL AND METHYL SALICYLATE	NATURES FORMULAE HEALTH PRODUCTS LTD.	d919b50a-5de2-1830-e053-2a95a90ab88d	2024-12-17	Warnings	Exact identifier application number: M017
Cold and Heat Lidocaine Patch Plus Menthol	LIDOCAINE, MENTHOL	Walgreen Company	1f262473-3f3c-4f3f-b507-590d06ff69a9	2024-12-17	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