Refresher

Product NDC: 69662-111
11-digit product format: 696620111
Labeler code: 69662
Product ID: 69662-111_37771115-d2fc-88e3-e063-6394a90aab56
Type: HUMAN OTC DRUG
Nonproprietary name: alcohol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Jao Limited
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-03-30
Substance: ALCOHOL
Active strength: 65 mL/100mL
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 · 12 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111-02	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111-04	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111-05	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111-03	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111-02	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111-04	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111-05	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111-01	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111-03	`bd6a592717d7…`	`303034d00443…`

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: Refresher
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALCOHOL	65 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
884783	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
1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
69662-111-01	2022-06-28	JAO Refresher
69662-111-01	2022-06-28	JAO Refresher
69662-111-02	2022-06-28	JAO Refresher
69662-111-02	2022-06-28	JAO Refresher
69662-111-03	2022-06-28	JAO Refresher
69662-111-03	2022-06-28	JAO Refresher
69662-111-04	2022-06-28	JAO Refresher
69662-111-04	2022-06-28	JAO Refresher
69662-111-05	2022-06-28	JAO Refresher
69662-111-05	2022-06-28	JAO Refresher
69662-111-01	2022-01-28	JAO Refresher
69662-111-01	2022-01-28	JAO Refresher
69662-111-02	2022-01-28	JAO Refresher
69662-111-02	2022-01-28	JAO Refresher
69662-111-03	2022-01-28	JAO Refresher
69662-111-03	2022-01-28	JAO Refresher
69662-111-04	2022-01-28	JAO Refresher
69662-111-04	2022-01-28	JAO Refresher
69662-111-05	2022-01-28	JAO Refresher
69662-111-05	2022-01-28	JAO Refresher

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69662-111-01	Refresher	236 mL in 1 BOTTLE, PUMP	LIQUID	236	15
69662-111-02	Refresher	59 mL in 1 BOTTLE, SPRAY	LIQUID	59	15
69662-111-03	Refresher	118 mL in 1 BOTTLE, SPRAY	LIQUID	118	15
69662-111-04	Refresher	3750 mL in 1 JUG	LIQUID	3750	15
69662-111-05	Refresher	840 mL in 1 POUCH	LIQUID	840	15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69662-111	REFRESHER (ALCOHOL) LIQUID [JAO LIMITED]	14	Current NDC, Legacy NDC, 5 package rows	20240105_1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8.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 43 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Surgical Scrub Brush/Sponge With Nail Cleaner	POVIDONE IODINE	Xinxiang Xinda Technology Co.,Ltd	12585502-c043-6ffb-e063-6394a90a6602	2026-01-08	Warnings	Exact identifier application number: M003
Thompson Alcohol	ISOPROPYL ALCOHOL	Thompson	f539db3b-f309-6a60-e053-2a95a90a5a9b	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-MICROBIAL	Unico International Trading Corp	a7d35899-8b70-14f0-e053-2995a90a5ce8	2026-01-08	Warnings	Exact identifier application number: M003
Germ Away	ANTI-MICROBIAL WIPE	Unico International Trading Corp	a6b4eec4-0b12-3a00-e053-2a95a90a7835	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-MICROBIAL	Unico International Trading Corp	a7d0ce42-9076-143c-e053-2995a90aeeb6	2026-01-08	Warnings	Exact identifier application number: M003
Wipex	ANTIBACTERIAL WIPE	Unico International Trading Corporation	261c7b8f-4adc-72ec-e063-6394a90a9211	2026-01-08	Warnings	Exact identifier application number: M003
Wipex	ANTIBACTERIAL WIPE	Unico International Trading Corporation	144453a2-8335-77be-e063-6394a90ab676	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-MICROBIAL	Unico International Trading Corp	a7d40204-3f69-7fb7-e053-2995a90a278b	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTIBACTERIAL HAND WIPE	Unico International Trading Corp	ad7d8546-d440-e661-e053-2a95a90a8fd3	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-MICROBIAL	Unico International Trading Corp	a7d47c07-12bd-3c8f-e053-2a95a90a9564	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-MICROBIAL	Unico International Trading Corp	a7d7f260-f5be-7940-e053-2995a90aaa03	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTIBACTERIAL	Unico International Trading Corp	ada02f20-07ef-9e90-e053-2995a90a0e8b	2026-01-08	Warnings	Exact identifier application number: M003
Germ-Away	ANTI-BACTERIAL	Unico International Trading Corp	adb59182-6541-2b35-e053-2a95a90a0f71	2026-01-08	Warnings	Exact identifier application number: M003
Castellani Paint 1.5%	PHENOL	The Podiatree Company	a10f18e0-b47c-424b-847e-bcc25aa250a4	2026-01-08	Warnings	Exact identifier application number: M003
Castellani Paint 1.5%	PHENOL	The Podiatree Company	5b8cff3c-71d2-418f-a43d-f570aa5408fd	2026-01-08	Warnings	Exact identifier application number: M003
Fortinia ID	PHENOL	The Podiatree Company	60c88eb7-22fe-4881-e053-2a91aa0a70ce	2026-01-08	Warnings	Exact identifier application number: M003
Gentian Violet 2%	GENTIAN VIOLET 2%	The Podiatree Company	60ba9bb0-cc7a-1ccf-e053-2a91aa0ac4b8	2026-01-08	Warnings	Exact identifier application number: M003
Isopropyl Rubbing Alcohol	ISOPROPYL ALCOHOL	NDC, Inc.	07bfadf4-7452-4c7a-b60e-feb658b92e73	2026-01-08	Warnings	Exact identifier application number: M003
Hydrogen Peroxide 3%	HYDROGEN PEROXIDE 3%	Epic Medical Supply Corp.	0da45476-46c3-428c-a2d9-70865d2b1277	2026-01-08	Warnings	Exact identifier application number: M003
Roll On Anti Perspirant Alcohol Free	ALUMINUM CHLOROHYDRATE	Medline Industries, LP	4f706801-dc2d-48c4-aa06-92207d86e55e	2026-01-08	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
884783	ethanol 65 % Topical Solution	PSN	1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8	15
884783	ethanol 0.65 ML/ML Topical Solution	SCD	1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8	15
884783	ethanol 65 % Topical Solution	SY	1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8	15

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69662-111-01	69662011101	236 mL in 1 BOTTLE, PUMP (69662-111-01)	236 ml	2016-04-06	0000-00-00	No	No	Current
69662-111-02	69662011102	59 mL in 1 BOTTLE, SPRAY (69662-111-02)	59 ml	2016-04-06	0000-00-00	No	No	Current
69662-111-03	69662011103	118 mL in 1 BOTTLE, SPRAY (69662-111-03)	118 ml	2016-05-04	0000-00-00	No	No	Current
69662-111-04	69662011104	3750 mL in 1 JUG (69662-111-04)	3750 ml	2017-07-20	0000-00-00	No	No	Current
69662-111-05	69662011105	840 mL in 1 POUCH (69662-111-05)	840 ml	2020-06-29	0000-00-00	No	No	Current