ITCH X

Product NDC: 0225-0495
11-digit product format: 002250495
Labeler code: 0225
Product ID: 0225-0495_2888be26-0ebc-ab78-e063-6394a90ada63
Type: HUMAN OTC DRUG
Nonproprietary name: BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE
Dosage form: GEL
Route: TOPICAL
Labeler: BF ASCHER AND CO INC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-09-19
Substance: BENZYL ALCOHOL; PRAMOXINE HYDROCHLORIDE
Active strength: 10; 1 g/100g; g/100g
Pharmacologic classes: Pediculicide [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: ITCH X
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZYL ALCOHOL	10 g/100g
PRAMOXINE HYDROCHLORIDE	1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
LKG8494WBH	Internal UNII lookup
88AYB867L5	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1293632	Internal RxNorm lookup
1293634	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
03c16d33-8f59-0184-e054-00144ff8d46c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8	Product name	1	20140508
9869efd7-d6dd-0665-5b67-53adbe6ef15e	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
0225-0495-33	ITCH X	35.4 g in 1 TUBE	GEL	35.4		6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0225-0495-33	GM - Gram	0225-0495	adf96dec-94ed-41d3-b853-e9b2a1ce7e47	1	2014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZYL ALCOHOL	ACTIVE INGREDIENT	LKG8494WBH	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
PRAMOXINE HYDROCHLORIDE	ACTIVE INGREDIENT	88AYB867L5	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
BENZYL ALCOHOL	ACTIVE MOIETY	LKG8494WBH	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
PRAMOXINE	ACTIVE MOIETY	068X84E056	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
ALOE	INACTIVE INGREDIENT	V5VD430YW9	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
BUTYLENE GLYCOL	INACTIVE INGREDIENT	3XUS85K0RA	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED)	INACTIVE INGREDIENT	Z135WT9208	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
DIAZOLIDINYL UREA	INACTIVE INGREDIENT	H5RIZ3MPW4	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
EDETOL	INACTIVE INGREDIENT	Q4R969U9FR	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0225-0495	ITCH X (BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE) GEL [BF ASCHER AND CO INC]	6	Current NDC, Legacy NDC, 1 package rows	20241208_03c16d33-8f59-0184-e054-00144ff8d46c.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 128 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Real Time Pain Relief Maxx Topical Analgesic	MENTHOL	REAL TIME PRODUCTS, INC	f45eb95a-2813-4124-bdb0-54e078a8237d	2024-08-20	Warnings	Exact identifier application number: M017
Theracare Lidocaine Pain relief	LIDOCAINE	Veridian Healthcare	1d8a3679-637d-94c0-e063-6294a90a9ecf	2024-08-19	Warnings	Exact identifier application number: M017
LidoSync	LIDOCAINE, MENTHOL	iON Pharma, LLC	200f883c-439a-3b99-e063-6394a90aed10	2024-08-19	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Oil Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	09243a23-1f17-f77b-e063-6394a90a0b22	2024-08-19	Warnings	Exact identifier application number: M017
CVS Health Maximum Strength Scalp Relief Anti-itch	HYDROCORTISONE	CVS Health	b5ef0005-8b76-4205-8be0-db3a7ed7d1c4	2024-08-19	Warnings	Exact identifier application number: M017
Rite Aid Pain Relieving Roll-On	LIDOCAINE HCL	Rite Aid Corporation	1406590c-667c-84eb-e063-6294a90a5052	2024-08-16	Warnings	Exact identifier application number: M017
Nuvira	CAPSAICIN 0.025%, MENTHOL 10%, METHYL NICOTINATE 0.25%, METHYL SALICYLATE 10%	Strand Health Group	ff448183-03cf-df2d-e053-6394a90a77f0	2024-08-16	Warnings	Exact identifier application number: M017
FLANAX	METHYL SALICYLATE, MENTHOL, CAPSAICIN	Belmora LLC	5e06c688-a086-4c1c-8dab-fcead61fef40	2024-08-13	Warnings	Exact identifier application number: M017
Pain Relief	MENTHOL	Pain Relieving Spray Inc.	1f44466f-044f-70fe-e063-6294a90ad575	2024-08-09	Warnings	Exact identifier application number: M017
Meijer Cold Therapy Pain Relieving	MENTHOL	Meijer Inc	1c5b55e3-f859-71b6-e063-6294a90a633b	2024-08-08	Warnings	Exact identifier application number: M017
HealthWise Soothing Cold Therapy Gel	MENTHOL 4%	Veridian Healthcare	1f09ccdd-09d8-6a8d-e063-6394a90a184f	2024-08-08	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Nantong Health & Beyond Hygienic Products Inc.	fbbbcc67-b46d-d41a-e053-6294a90aa55d	2024-08-08	Warnings	Exact identifier application number: M017
Cheezheng Pain Relief Cream	MENTHOL	Tibet Cheezheng Tibetan Medicine Co. Ltd	37279a3f-9207-4e4c-90d6-52735044f104	2024-08-07	Warnings	Exact identifier application number: M017
CVS Health Hydrocortisone Anti Itch	HYDROCORTISONE	CVS Health	546a1b8a-8254-432a-85c4-38ebee5ad568	2024-08-07	Warnings	Exact identifier application number: M017
SANTO REMEDIO Alivio Pain Relieving Lavender Scent	LIDOCAINE HYDROCHLORIDE, MENTHOL	SANTO REMEDIO LLC	ab53c7f2-a768-4f36-89d6-e128a1a940c2	2024-08-05	Warnings	Exact identifier application number: M017
CVS Health Maximum Strength Hydrocortisone	HYDROCORTISONE OINTMENT	CVS Health	ee9ed7ca-1642-4cf6-ae4b-d1c11b37eaf3	2024-08-02	Warnings	Exact identifier application number: M017
Anti-Itch Vulva Cream 1 Hydrocortisone Acetate	HYDROCORTISONE ACETATE	The Honey Pot Company LLC	6f32b536-6ebf-49a8-abb6-2a1daae2f6d7	2024-08-01	Warnings	Exact identifier application number: M017
Anti Itch Soothing 1 Pramoxine Hydrochloride	PRAMOXINE HYDROCHLORIDE	The Honey Pot Company LLC	8bfeea34-25d5-4721-a17f-d9f1d0084cc3	2024-08-01	Warnings	Exact identifier application number: M017
AVON footworks Arthritis Achy Foot and Muscle	METHYL SALICYLATE	The Avon Company	1f440f60-cfc4-511e-e063-6294a90a87db	2024-08-01	Warnings	Exact identifier application number: M017
AVON footworks Maximum Strength Cracked Heel	BENZALKONIUM CHLORIDE, LIDOCAINE	The Avon Company	1f45752e-4a55-431e-e063-6294a90aa57a	2024-08-01	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LKG8494WBH	BENZYL ALCOHOL	100-51-6	BENZYL ALCOHOL
88AYB867L5	PRAMOXINE HYDROCHLORIDE	637-58-1	PRAMOXINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1293634	Itch-X 10 % / 1 % Topical Gel	PSN	03c16d33-8f59-0184-e054-00144ff8d46c	6
1293632	pramoxine HCl 1 % / benzyl alcohol 10 % Topical Gel	PSN	03c16d33-8f59-0184-e054-00144ff8d46c	6
1293634	benzyl alcohol 0.1 ML/ML / pramoxine hydrochloride 0.01 MG/MG Topical Gel [Itch-X]	SBD	03c16d33-8f59-0184-e054-00144ff8d46c	6
1293632	benzyl alcohol 0.1 ML/ML / pramoxine hydrochloride 0.01 MG/MG Topical Gel	SCD	03c16d33-8f59-0184-e054-00144ff8d46c	6
1293632	benzyl alcohol 10 % / pramoxine hydrochloride 1 % Topical Gel	SY	03c16d33-8f59-0184-e054-00144ff8d46c	6
1293634	Itch-X (benzyl alcohol 10 % / pramoxine hydrochloride 1 % ) Topical Gel	SY	03c16d33-8f59-0184-e054-00144ff8d46c	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0225-0495-33	00225049533	35.4 g in 1 TUBE (0225-0495-33)	35.4 g	2014-09-19	0000-00-00	No	No	Current