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 114 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Henry Schein Povidone-Iodine Swabsticks	POVIDONE-IODINE	Henry Schein, Inc.	5854f241-6cfc-4e5a-ba72-92dd0703f728	2023-10-13	Warnings	Exact identifier application number: M003
DawnMist Alcohol Hand Sanitizer	ALCOHOL	Dukal LLC	a2df96a9-8514-6839-e053-2a95a90a9417	2023-10-13	Warnings	Exact identifier application number: M003
DUKAL STING RELIEF PAD	BENZOCAINE	Dukal LLC	67c1ddc7-8fde-4431-84cb-f757682d5f3e	2023-10-13	Warnings	Exact identifier application number: M003
First Aid Only First Aid/Burn	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	Acme United Corporation	07245b54-b193-178e-e063-6394a90a2581	2023-10-09	Warnings	Exact identifier application number: M003
Hand sanitizer 2oz 2pk original	ETHYL ALCOHOL	Rejoice International Corp.	06dc1730-216a-8b4d-e063-6294a90a4184	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 1.8oz with extra clip original	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	06dcf8dc-0831-475e-e063-6394a90a9fef	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 2oz 2pk original	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	06dd2427-097c-b0fa-e063-6294a90a4f82	2023-10-04	Warnings	Exact identifier application number: M003
Hand sanitizer 1.8oz with extra clip original	ETHYL ALCOHOL	Rejoice International Corp.	06da0cc1-95f2-4f88-e063-6394a90a25ea	2023-10-03	Warnings	Exact identifier application number: M003
First Aid Antiseptic Alcohol Pads Isopropyl Alcohol 70 Rite Aid	ISOPROPYL ALCOHOL	Rite Aid Corporation	aa0df5fe-62d1-407d-b8f9-a7fd9473d569	2023-10-02	Warnings	Exact identifier application number: M003
Foaming Instant Hand Sanitizer with Aloe	ETHANOL	MCKESSON MEDICAL-SURGICAL INC.	5c1f69b7-c8d8-477c-b614-47a3287b0e4c	2023-06-05	Warnings	Exact identifier application number: M003
Bactine Max Dry	LIDOCAINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	466404cd-c46a-4944-b1ac-3b3b17f436a1	2022-12-27	Warnings	Exact identifier application number: M003
Povidone-Iodine Pad	POVIDONE-IODINE	Shandong Haiyan Medical Manufacture Co., Ltd.	c9187a07-92d5-15ac-e053-2995a90af4cb	2022-03-19	Warnings	Exact identifier application number: M003
Alcohol Prep Pad	ISOPROPYL ALCOHOL	Shandong Haiyan Medical Manufacture Co., Ltd.	1a117840-22d0-4a88-b1a6-e43162a444ab	2022-03-19	Warnings	Exact identifier application number: M003
FIRSTAR BZK Antiseptic Towelette	BENZALKONIUM CHLORIDE	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	28591a97-9291-48c8-a8e3-c419180331b3	2021-07-06	Warnings	Exact identifier application number: M003
Bactine Max	BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE	WellSpring Pharmaceutical Corporation	28e8a311-20a4-45a1-8d5d-ca42b101c275	2021-02-24	Warnings	Exact identifier application number: M003
Hand Sanitizer Lemon 2oz	ALCOHOL	Ningbo Rejoice International	b0a4159a-cb07-4ce6-e053-2995a90a76e7	2020-10-02	Warnings	Exact identifier application number: M003
Sanix Alcohol Hand Rub	ALCOHOL	Topiderm, Inc	a4fbb714-4f20-400a-ab98-f1c8807ce6fc	2020-03-24	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