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 32 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Universal Rubbing Alcohol	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	183efdc2-cf3e-4f06-b292-0cfd097418b3	2026-02-23	Warnings	Exact identifier application number: M003
Konix Povidone Iodine Topical Antiseptic	POVIDONE-IODINE	TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS	0cc6b001-4982-40ee-a476-151f86c14a8e	2026-02-19	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Save-A-Lot Food Stores Ltd	e279b23d-6779-4f04-a93c-1c2a49559639	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Meijer, Inc.	193292da-390b-4430-91b1-1d159ac50507	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	Meijer, Inc.	4989f1cd-4555-405a-a5f8-8714d472983c	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M003
First Aid Antiseptic	POVIDONE-IODINE	Target Corporation	78693ec1-d725-408c-bb95-2261faad84ac	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M003
Travel Wipes Fresh Citrus Scent	ALCOHOL	SINGULAR ENTERPRISES LLC	ea77be5e-7c69-4787-b39a-4753b002dbbd	2026-02-18	Warnings	Exact identifier application number: M003
Travel Wipes Unscented	ISOPROPYL ALCOHOL	SINGULAR ENTERPRISES LLC	dd046146-fda7-438c-98ca-96ea1dd0ae0b	2026-02-18	Warnings	Exact identifier application number: M003
Benzalkonium chloride	FIRST AID ANTISEPTIC FOAM	Target Corporation	4599eb25-2877-fc62-e063-6294a90a5d18	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M003
Konix Povidone Iodine Topical Antiseptic	POVIDONE-IODINE	TURKUAZ SAGLIK HIZMETLERI MEDIKAL TEMIZLIK KIMYASAL URUNLER SANAYI VE TICARET AS	8a9848b0-19df-455a-9984-5ea2e5ce1b9f	2026-02-17	Warnings	Exact identifier application number: M003
Wintergreen 91 - Iron Lab	ETHYL ALCOHOL	Iron Lab SA de CV	323a0717-0d61-c911-e063-6394a90a4854	2026-02-17	Warnings	Exact identifier application number: M003
Ethyl Rubbing Alcohol	ALCOHOL	Iron Lab SA de CV	323b2f5d-34b9-8f5b-e063-6394a90a59d5	2026-02-17	Warnings	Exact identifier application number: M003
50 Ethyl Rubbing Alcohol	ALCOHOL	Iron Lab SA de CV	323b7ff8-91ce-c7a4-e063-6394a90a69fc	2026-02-17	Warnings	Exact identifier application number: M003
70 Alcohol Hand Sanitizer	ALCOHOL	Iron Lab SA de CV	323c06d5-c984-39b8-e063-6294a90a0d3f	2026-02-17	Warnings	Exact identifier application number: M003
50 Wintergreen Alcohol	ALCOHOL	Iron Lab SA de CV	323baeb1-e3ee-ec70-e063-6294a90a30f0	2026-02-17	Warnings	Exact identifier application number: M003
70 Rubbing Ethyl Alcohol	ALCOHOL	Iron Lab SA de CV	323be8b4-4588-e2a6-e063-6394a90ab68b	2026-02-17	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	United Natural Foods, Inc. dba UNFI	8a44aa29-58d6-4971-b572-4579f03ed227	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M003
INSTACLEAN HAND SANITIZING	ALCOHOL	SHIELD LINE LLC	6d606fae-d95e-cffc-e053-2991aa0a988b	2026-02-17	Warnings	Exact identifier application number: M003
Burn Cream	BENZALKONIUM CHLORIDE, LIDOCAINE HCI	Trifecta Pharmaceuticals USA LLC	087ac43c-1076-d1e2-e063-6294a90a5859	2026-02-16	Warnings	Exact identifier application number: M003
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Valu Merchandisers Company	a631c976-cb9b-4099-8630-2a10c14bd3bd	2026-02-16	Warnings, Adverse reactions	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