Kleenex Ultra Moisturizing Hand Sanitizer

Product NDC: 55118-530
11-digit product format: 551180530
Labeler code: 55118
Product ID: 55118-530_92ebe19a-e5cd-40cb-89ec-60d675a726d3
Type: HUMAN OTC DRUG
Nonproprietary name: Alcohol
Dosage form: SOLUTION
Route: TOPICAL
Labeler: Kimberly-Clark Corporation
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-03-01
Substance: ALCOHOL
Active strength: 70 mL/100mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 5 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded package	package	55118-530	55118-530-10	D	Discontinued by firm	2026-10-20
excluded package	package	55118-530	55118-530-11	D	Discontinued by firm	2026-10-20
excluded package	package	55118-530	55118-530-12	D	Discontinued by firm	2026-10-20
excluded package	package	55118-530	55118-530-88	D	Discontinued by firm	2026-10-20
excluded package	package	55118-530	55118-530-99	D	Discontinued by firm	2026-10-20

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 · 42 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55118-530-11	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55118-530-10	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55118-530-88	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55118-530-99	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	55118-530-12	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55118-530-11	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55118-530-10	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55118-530-88	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55118-530-99	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	55118-530-12	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55118-530-11	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55118-530-10	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55118-530-88	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55118-530-99	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	55118-530-12	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55118-530-11	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55118-530-10	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55118-530-88	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55118-530-99	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	55118-530-12	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	55118-530-11	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	55118-530-10	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	55118-530-88	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	55118-530-99	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	55118-530-12	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	55118-530-11	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	55118-530-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	55118-530-88	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	55118-530-99	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	55118-530-12	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	55118-530-11	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	55118-530-12	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	55118-530-88	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	55118-530-99	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	55118-530-10	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

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: Kleenex Ultra Moisturizing Hand Sanitizer
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	70 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3K9958V90M	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
616805	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
75e884bf-8e0d-41e7-adbb-4400ee3d1e07	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
55118-530-10	2022-12-14	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-11	2022-12-14	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-12	2022-12-14	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-88	2022-12-14	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-99	2022-12-14	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-10	2020-01-31	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-11	2020-01-31	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-12	2020-01-31	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-88	2020-01-31	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer
55118-530-99	2020-01-31	KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55118-530-10	Kleenex Ultra Moisturizing Hand Sanitizer	1000 mL in 1 BAG	SOLUTION	1000	8
55118-530-11	Kleenex Ultra Moisturizing Hand Sanitizer	44 mL in 1 BOTTLE, PLASTIC	SOLUTION	44	8
55118-530-12	Kleenex Ultra Moisturizing Hand Sanitizer	1200 mL in 1 BAG	SOLUTION	1200	8
55118-530-63	Kleenex Ultra Moisturizing Hand Sanitizer	6 in 1 CARTON	SOLUTION	6	8
55118-530-65	Kleenex Ultra Moisturizing Hand Sanitizer	2 in 1 CARTON	SOLUTION	2	8
55118-530-88	Kleenex Ultra Moisturizing Hand Sanitizer	236 mL in 1 BOTTLE, PLASTIC	SOLUTION	236	8
55118-530-91	Kleenex Ultra Moisturizing Hand Sanitizer	1000 mL in 1 BOTTLE	SOLUTION	1000	8
55118-530-92	Kleenex Ultra Moisturizing Hand Sanitizer	1200 mL in 1 BOTTLE	SOLUTION	1200	8
55118-530-99	Kleenex Ultra Moisturizing Hand Sanitizer	472 mL in 1 BOTTLE, PLASTIC	SOLUTION	472	8

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Alcohol	ACTIVE INGREDIENT	3K9958V90M	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Alcohol	ACTIVE MOIETY	3K9958V90M	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Aloe Vera Leaf	INACTIVE INGREDIENT	ZY81Z83H0X	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Betaine	INACTIVE INGREDIENT	3SCV180C9W	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Camellia Oleifera Leaf	INACTIVE INGREDIENT	5077EL0C60	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Citric Acid Monohydrate	INACTIVE INGREDIENT	2968PHW8QP	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Cucumber	INACTIVE INGREDIENT	YY7C30VXJT	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Isopropyl Alcohol	INACTIVE INGREDIENT	ND2M416302	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Panthenol	INACTIVE INGREDIENT	WV9CM0O67Z	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55118-530	KLEENEX ULTRA MOISTURIZING HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]	6	Current NDC, Legacy NDC, 9 package rows	20241215_75e884bf-8e0d-41e7-adbb-4400ee3d1e07.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 2 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walmart	ISOPROPYL ALCOHOL	Walmart, Inc.	2eff98ba-5736-b07e-e063-6394a90aeea9	2026-09-04	Warnings	Exact identifier application number: M003
Walgreen Alcohol	ISOPROPYL ALCOHOL	Walgreens Company	deeae1ea-3d81-4260-95be-c4f328e3fdef	2026-09-04	Warnings	Exact identifier application number: M003
Dollar General	ISOPROPYL ALCOHOL	Dollar General Corporation	00b2ef34-42d9-523c-e063-6294a90a753d	2026-09-03	Warnings	Exact identifier application number: M003
Signature Select Alcohol Prep Pads	ISOPROPYL ALCOHOL	Better Living Brands LLC	31ce72e3-03a3-1608-e063-6394a90ad850	2026-09-03	Warnings	Exact identifier application number: M003
SurviveX Sting Relief	STING RELIEF WIPE	Changzhou Maokang Medical Products Co., Ltd.	5a83b1f1-c8dc-cf07-e063-6394a90a20ca	2026-09-03	Warnings	Exact identifier application number: M003
Benzethonium chloride Plus Dyclonine hydrochloride	LIQUID BANDAGE	Kroger Co.	fe604470-917f-4cbd-a1e6-ac1dc7c57ff6	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	Rite Aid Corporation	5104f9ab-0b28-449f-a55a-5438713a24df	2026-09-02	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	UpLift Brands, LLC	5a81b635-d188-0b29-e063-6294a90a1e4b	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	CVS Pharmacy, Inc.	7f518646-c8fe-499a-b5e4-8e5a5a90e01d	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	The Kroger Company	6551187f-5cde-4149-931f-b057bd760750	2026-09-02	Warnings	Exact identifier application number: M003
Unscented NasalGuard Antiseptic Topical	BENZALKONIUM CHLORIDE	TRUTEK CORP.	eb036e11-a28c-fdc0-e053-2a95a90a9cdb	2026-09-02	Warnings	Exact identifier application number: M003
Harris Teeter	ISOPROPYL ALCOHOL	Harris Teeter, LLC	d2bb20bd-ec83-8d80-e053-2a95a90a2bba	2026-09-02	Warnings	Exact identifier application number: M003
School Health	ISOPROPYL ALCOHOL	School Health Corporation	db5d0b22-f2d7-23e5-e053-2a95a90aeb51	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Topco Associates	2642298f-607e-fdca-e063-6394a90a69d9	2026-09-02	Warnings	Exact identifier application number: M003
HUSTLE BUTTER NUMBING	LIDOCAINE HCL, BENZALKONIUM CHLORIDE	H.B.D. DIST. INC.	5b4d0390-dac6-4a71-9fdc-5c31543e7c5a	2026-09-02	Warnings	Exact identifier application number: M003
NasalGuard Antiseptic Topical Cool Menthol	BENZALKONIUM CHLORIDE	TRUTEK CORP.	e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8	2026-09-01	Warnings	Exact identifier application number: M003
Maximum Strength Betadine Clear	BENZALKONIUM CL AND PRAMOXINE HCL	Atlantis Consumer Healthcare, Inc.	31b94a76-1536-47c0-ab03-e487c2625c58	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a28101f-ea8e-6071-e063-6294a90aad91	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a3e62ce-52dc-121b-e063-6294a90a898f	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a49db18-c270-6f46-e063-6294a90afb5d	2026-08-31	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3K9958V90M	ALCOHOL	64-17-5	ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
616805	ethanol 70 % Topical Foam	PSN	75e884bf-8e0d-41e7-adbb-4400ee3d1e07	8
616805	ethanol 0.7 ML/ML Topical Foam	SCD	75e884bf-8e0d-41e7-adbb-4400ee3d1e07	8
616805	ethanol 70 % Topical Foam	SY	75e884bf-8e0d-41e7-adbb-4400ee3d1e07	8

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55118-530-10	55118053010	1000 mL in 1 BAG (55118-530-10)	1000 ml	2012-03-01	0000-00-00	No	No	Current
55118-530-11	55118053011	44 mL in 1 BOTTLE, PLASTIC (55118-530-11)	44 ml	2012-03-01	0000-00-00	No	No	Current
55118-530-12	55118053012	1200 mL in 1 BAG (55118-530-12)	1200 ml	2012-03-01	0000-00-00	No	No	Current
55118-530-63	55118053063	6 BOTTLE in 1 CARTON (55118-530-63) / 1000 mL in 1 BOTTLE (55118-530-91)	6 bottle	2015-03-01		No	No	Current
55118-530-65	55118053065	2 BOTTLE in 1 CARTON (55118-530-65) / 1200 mL in 1 BOTTLE (55118-530-92)	2 bottle	2015-03-01		No	No	Current
55118-530-88	55118053088	236 mL in 1 BOTTLE, PLASTIC (55118-530-88)	236 ml	2012-03-01	0000-00-00	No	No	Current
55118-530-91	55118053091	1000 mL in 1 BOTTLE	1000 ml					Historical
55118-530-92	55118053092	1200 mL in 1 BOTTLE	1200 ml					Historical
55118-530-99	55118053099	472 mL in 1 BOTTLE, PLASTIC (55118-530-99)	472 ml	2012-03-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
KLEENEX ® ULTRA Moisturizing Foam Hand Sanitizer	Kimberly-Clark Corporation \| Hubot CDMO \| Cyan Labs	2026-05-08	HUMAN OTC DRUG LABEL	8