Hand sanitizer 2oz 2pk with aloe vera

Product NDC: 75742-022
11-digit product format: 757420022
Labeler code: 75742
Product ID: 75742-022_47afd8f9-9abf-f8ff-e063-6394a90aff33
Type: HUMAN OTC DRUG
Nonproprietary name: Ethyl Alcohol 70%
Dosage form: GEL
Route: TOPICAL
Labeler: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-09-10
Substance: ALCOHOL
Active strength: 70 mL/100mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 27 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	75742-022-02	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	75742-022-01	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	75742-022-02	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	75742-022-01	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	75742-022-02	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	75742-022-01	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	75742-022-02	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	75742-022-01	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	75742-022-02	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	75742-022-01	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	75742-022-02	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	75742-022-01	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75742-022-01	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	75742-022-02	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75742-022-01	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	75742-022-02	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75742-022-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	75742-022-02	U	Excluded because listing certification expired	`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: Hand sanitizer 2oz 2pk with aloe vera
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
581662	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
04fe378d-ee1e-ad52-e063-6294a90ae146	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
75742-022-01	2026-01-05	04fe378d-ee1e-ad52-e063-6294a90ae146
75742-022-02	2026-01-05	04fe378d-ee1e-ad52-e063-6294a90ae146
75742-022-01	2025-01-30	04fe378d-ee1e-ad52-e063-6294a90ae146
75742-022-02	2025-01-30	04fe378d-ee1e-ad52-e063-6294a90ae146

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75742-022-01	Hand sanitizer 2oz 2pk with aloe vera	59 mL in 1 BOTTLE	GEL	59	2
75742-022-02	Hand sanitizer 2oz 2pk with aloe vera	59 mL in 1 BOTTLE	GEL	59	2
75742-022-02	Hand sanitizer 2oz 2pk with aloe vera	2 in 1 BOX	GEL	2	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75742-022	HAND SANITIZER 2OZ 2PK WITH ALOE VERA (ETHYL ALCOHOL 70%) GEL [ZHEJIANG GUOYAO JINGYUE AEROSOL CO., LTD.]	1	Current NDC, 3 package rows	20230911_04fe378d-ee1e-ad52-e063-6294a90ae146.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 45 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antiseptic Cleaning wipe	ANTISEPTIC CLEANING WIPE	SHENZHEN BENLIJU BIO-TECH CO.,LTD	203d01ae-d99e-bce3-e063-6294a90a1a2d	2026-01-05	Warnings	Exact identifier application number: M003
Povidone-lodine prep pad	POVIDONE-LODINE PREP PAD	SHENZHEN BENLIJU BIO-TECH CO.,LTD	201545b8-0697-5601-e063-6394a90a12f4	2026-01-05	Warnings	Exact identifier application number: M003
Sting Relief prep Pad	STING RELIEF PREP PAD	SHENZHEN BENLIJU BIO-TECH CO.,LTD	202c7b77-1a48-52a5-e063-6394a90a2eb2	2026-01-05	Warnings	Exact identifier application number: M003
Skin Cleaning Care Wipes	SKIN CLEANING CARE WIPES	SHENZHEN BENLIJU BIO-TECH CO.,LTD	203d7a95-65fe-ca65-e063-6294a90acc6e	2026-01-05	Warnings	Exact identifier application number: M003
ANTISEPTIC CLEANSING WIPE(0.9% NACL)	ANTISEPTIC CLEANSING WIPE(0.9% NACL)	SHENZHEN BENLIJU BIO-TECH CO.,LTD	33e1c026-8a35-a47a-e063-6294a90a2406	2026-01-05	Warnings	Exact identifier application number: M003
Hand Sanitizing Wipes	HAND SANITIZING WIPES	SHENZHEN BENLIJU BIO-TECH CO.,LTD	37487da6-4e0e-6625-e063-6394a90a0af1	2026-01-05	Warnings	Exact identifier application number: M003
Hand wipes	HAND WIPES	SHENZHEN BENLIJU BIO-TECH CO.,LTD	39f3acca-7275-88ca-e063-6394a90ad1a2	2026-01-05	Warnings	Exact identifier application number: M003
Smart Care Hand Sanitizer Vanilla Heaven	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	47a0781b-9b25-f04b-e063-6294a90ae7e5	2026-01-05	Warnings	Exact identifier application number: M003
Smart Care Hand Sanitizer Berry	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	47a16397-dff3-7d79-e063-6394a90a040f	2026-01-05	Warnings	Exact identifier application number: M003
IDOSWAB B	ISOPROPYL ALCOHOL	IDO PHARM	16d19630-b67a-f3e1-e063-6394a90a7429	2026-01-05	Warnings	Exact identifier application number: M003
Sure Comfort Alcohol Prep Pads	ISOPROPYL ALCOHOL	IDO PHARM	27def94b-d3a6-18b7-e063-6394a90a22a6	2026-01-05	Warnings	Exact identifier application number: M003
Smart Care Hand Sanitizer Lemon Lime	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	47aeaae9-740d-a28a-e063-6294a90a6460	2026-01-05	Warnings	Exact identifier application number: M003
Smart Care Hand Sanitizer Calming Lavender	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	47aeeef9-0eed-e7d0-e063-6394a90a6d31	2026-01-05	Warnings	Exact identifier application number: M003
Smart Care Hand Sanitizer Coconut Breeze	ALCOHOL	Shenzhen Lantern Scicence Co.,Ltd.	47af27a7-3df9-270a-e063-6394a90abc7d	2026-01-05	Warnings	Exact identifier application number: M003
Hand Sanitiser	ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a44d82bf-68a3-56bc-e053-2995a90ae526	2026-01-05	Warnings	Exact identifier application number: M003
Green Island Sanitiser	ALCOHOL	Zhejiang Guoyao Aerosol Co., Ltd	a7d1df16-3566-badf-e053-2a95a90aa61a	2026-01-05	Warnings	Exact identifier application number: M003
Green Island	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a7443a72-6ee5-07f7-e053-2995a90a3341	2026-01-05	Warnings	Exact identifier application number: M003
SHABOINK	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a8bc5da3-8660-6343-e053-2995a90ac905	2026-01-05	Warnings	Exact identifier application number: M003
SHABOINK	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a8c0c9ce-05ac-0f33-e053-2a95a90ab8ed	2026-01-05	Warnings	Exact identifier application number: M003
H2One	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a9bcecf7-7767-69b4-e053-2995a90a9247	2026-01-05	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
581662	ethanol 70 % Topical Gel	PSN	04fe378d-ee1e-ad52-e063-6294a90ae146	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	04fe378d-ee1e-ad52-e063-6294a90ae146	2
581662	ethanol 70 % Topical Gel	SY	04fe378d-ee1e-ad52-e063-6294a90ae146	2
581662	ethyl alcohol 70 % Topical Gel	SY	04fe378d-ee1e-ad52-e063-6294a90ae146	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
75742-022-01	75742002201	59 mL in 1 BOTTLE (75742-022-01)	59 ml	2023-09-10	No	No	Current
75742-022-02	75742002202	2 BOTTLE in 1 BOX (75742-022-02) / 59 mL in 1 BOTTLE	2 bottle	2023-09-10	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Ethyl Alcohol 70% - Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	2026-01-05	HUMAN OTC DRUG LABEL	2