Family Care Maximum Strength Medicated Anti Itch

Product NDC: 65923-104
11-digit product format: 659230104
Labeler code: 65923
Product ID: 65923-104_41b455e2-0768-80cb-e063-6394a90a5698
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: CREAM
Route: TOPICAL
Labeler: United Exchange Corp.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-11-24
Substance: MENTHOL; PRAMOXINE HYDROCHLORIDE
Active strength: 10; 10 mg/g; mg/g
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: Family Care Maximum Strength Medicated Anti Itch
Listing expiration: 2026-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
88AYB867L5	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
430b5753-3087-4cb1-bf54-0eedc3f4b1d5	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
65923-104-14	Family Care Maximum Strength Medicated Anti Itch	1 in 1 CARTON	CREAM	1		16
65923-104-14	Family Care Maximum Strength Medicated Anti Itch	14 g in 1 TUBE	CREAM	14		16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
PRAMOXINE HYDROCHLORIDE	ACTIVE INGREDIENT	88AYB867L5	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
PRAMOXINE	ACTIVE MOIETY	068X84E056	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
CARBOMER HOMOPOLYMER TYPE C	INACTIVE INGREDIENT	4Q93RCW27E	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
GLYCERYL MONOSTEARATE	INACTIVE INGREDIENT	230OU9XXE4	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
MINERAL OIL	INACTIVE INGREDIENT	T5L8T28FGP	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
POLYSORBATE 60	INACTIVE INGREDIENT	CAL22UVI4M	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
STEARYL ALCOHOL	INACTIVE INGREDIENT	2KR89I4H1Y	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6
WATER	INACTIVE INGREDIENT	059QF0KO0R	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP]	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65923-104	FAMILY CARE MAXIMUM STRENGTH MEDICATED ANTI ITCH (MENTHOL) CREAM [UNITED EXCHANGE CORP.]	14	Current NDC, Legacy NDC, 2 package rows	20250305_430b5753-3087-4cb1-bf54-0eedc3f4b1d5.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 88 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tattoo	TATTOO CREAM	Perfso (HK) Co., Limited	39773cab-12df-4520-e063-6294a90abc5b	2025-07-08	Warnings	Exact identifier application number: M017
Neutrogena Sun Rescue After Sun Medicated Relief	CAMPHOR (SYNTHETIC)	Kenvue Brands LLC	c95c5b64-b90f-1143-e053-2a95a90aa03c	2025-07-07	Warnings	Exact identifier application number: M017
sunmark Hydrocortisone	HYDROCORTISONE	Strategic Sourcing Services LLC	210079e9-3d2f-4489-b468-b96b145034ed	2025-07-07	Warnings	Exact identifier application number: M017
Relief Gel	LIDOCAINE HCL	Good Clean Love, Inc.	e5fa2265-ccb7-750c-e053-2995a90aa51e	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone Plus 12 Moisturizers	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	09ac2749-a60f-4039-8c80-a0d2eaf50c34	2025-07-07	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	2ada9ec2-1c28-4da2-8639-07b3193ffb32	2025-07-03	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE	Sun Pharmaceutical Industries, Inc.	caa2fd64-e262-4d7c-ad8a-69f506feba8c	2025-07-03	Warnings	Exact identifier application number: M017
Stopain Extra Strength	MENTHOL	Troy Manufacturing, Inc.	07e9a235-6d10-4407-8729-beaf936e97ad	2025-07-03	Warnings	Exact identifier application number: M017
Blue Ice Topical Analgesic Gel	ICE GEL	International Wholesale	397cd306-078d-5b7d-e063-6294a90a8bbc	2025-07-03	Warnings	Exact identifier application number: M017
LIDOCAINE	LIDOCAINE, MENTHOL	Vive Health LLC	236ccc6d-21b7-6153-e063-6394a90a4634	2025-07-02	Warnings	Exact identifier application number: M017
AsperFlex MAX	LIDOCAINE 4% WITH MENTHOL 1%	Akron Pharma Inc.	ccf6172b-350a-4b78-b844-f84bf17c491f	2025-07-02	Warnings	Exact identifier application number: M017
METHYL SALICYLATE 25%	METHYL SALICYLATE	Oncora Pharma, LLC	3766e3a9-94a8-4c3e-e063-6394a90aa24a	2025-07-01	Warnings	Exact identifier application number: M017
Diphenhydramine Hydrochloride and Zinc Acetate	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Sun Pharmaceutical Industries, Inc.	c89e3de8-7d71-485c-8fc5-2832d6024f16	2025-07-01	Warnings	Exact identifier application number: M017
Westlake Outdoor Pain and Itch Relieving	LIDOCAINE 4% PAIN AND ITCH RELIEVING	WESTLAKE HB PHARMA	3c563b28-4f4f-9d0c-e063-6294a90adf73	2025-07-01	Warnings	Exact identifier application number: M017
Cortizone 10 Water Resistant	HYDROCORTISONE	Chattem, Inc.	118e55e7-241f-44c4-959e-09bf6221bd77	2025-07-01	Warnings	Exact identifier application number: M017
Quit Smoking Nicotine Patches	NICOTINE TRANSDERMAL PATCHES	Shenzhen Paxi Trading Co., Ltd.	38c1616e-3b09-0669-e063-6294a90a2c86	2025-06-29	Warnings	Exact identifier application number: M017
Plantar Fasciitis Cream	CAMPHOR	SOLALIA LLC	388f33c2-2bdf-ded8-e063-6294a90aeeac	2025-06-27	Warnings	Exact identifier application number: M017
4 Lidocaine Topical Anesthetic	LIDOCAINE	RUGBY LABORATORIES	63327e57-f4c8-4ae6-9d28-cef8697bbdcc	2025-06-27	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	ANTI-ITCH CONTINUOUS SPRAY	Wal-Mart Stores, Inc.	709c3bb8-5b36-4823-941a-45ddb3e431c4	2025-06-27	Warnings	Exact identifier application number: M017
Burn Relief Professional Bio-Kool	LIDOCAINE - 4%	Kool-Down Inc.	827e9c69-4706-0ccf-e053-2991aa0aa1c1	2025-06-27	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1116155	menthol 1 % / pramoxine HCl 1 % Topical Cream	PSN	430b5753-3087-4cb1-bf54-0eedc3f4b1d5	16
1116155	menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream	SCD	430b5753-3087-4cb1-bf54-0eedc3f4b1d5	16
1116155	menthol 1 % / pramoxine hydrochloride 1 % Topical Cream	SY	430b5753-3087-4cb1-bf54-0eedc3f4b1d5	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
65923-104-14	65923010414	1 TUBE in 1 CARTON (65923-104-14) / 14 g in 1 TUBE	1 tube	2018-10-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Family Care Anti-Itch + Pain Relief Cream 0.5oz (10497)	United Exchange Corp.	2025-10-21	HUMAN OTC DRUG LABEL	16