Refresher

Product NDC: 69662-111
Requested package NDC: 69662-111-01
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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	69662-111	69662-111-01	I	Inactivated by FDA		excluded / ndc_excluded.zip	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	69662-111	69662-111-01	I	Inactivated by FDA		excluded / ndc_excluded.zip	`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 38 of 114 · 2,277 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
New Skin Bandage	BENZETHONIUM CHLORIDE	Advantice Health, LLC	60996119-8367-4e22-b6ec-c36490635fa4	2026-01-28	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	1409c437-ff17-481d-94be-87dd6d463ba9	2026-01-28	Warnings	Exact identifier application number: M003
Singular Wipes Unscented	ISOPROPYL ALCOHOL	SINGULAR ENTERPRISES LLC	ac2b352f-6cb2-4683-bb41-13e8ecb186bf	2026-01-27	Warnings	Exact identifier application number: M003
Singular Wipes fresh Citrus Scent	ALCOHOL	SINGULAR ENTERPRISES LLC	867a25d2-3d2c-4dad-bbe8-84195c03a87d	2026-01-27	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	4906f079-8c9f-e3b0-e063-6294a90ad0f8	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	4912b681-e21a-1ddf-e063-6294a90aa9f4	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	491a6d77-8a84-c76d-e063-6394a90ac61f	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	491b55ca-2c7a-0eb7-e063-6394a90a9cb7	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	491c4af8-c699-7128-e063-6294a90ae0f9	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	491de8ca-07e7-0aa3-e063-6394a90ae36f	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	492793db-7dc2-8313-e063-6394a90a52bf	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	4928615e-d1a9-72b8-e063-6394a90aa7ed	2026-01-26	Warnings	Exact identifier application number: M003
Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	4943e51a-bb8e-745a-e063-6294a90a0a3d	2026-01-26	Warnings	Exact identifier application number: M003
Hand sanitizer	HAND SANITIZER SPRAY	Beimei Biotechnology (Guangzhou) Co., Ltd.	49455156-1072-14f5-e063-6294a90abdff	2026-01-26	Warnings	Exact identifier application number: M003
Anti-bacterial Hand Wipes	ANTI-BACTERIAL HAND WIPES	Jinhua Aidi Daily Chemical Co., Ltd.	494b09a4-4982-13bf-e063-6394a90a486f	2026-01-26	Warnings	Exact identifier application number: M003
Homworks Alcohol Wipes Multipurpose	ETHYL ALCOHOL	Acadian Crossing Consumer Products, LLC.	c9f0c3b3-5f39-dfa6-e053-2995a90a7644	2026-01-26	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	87288939-cc34-4437-94ab-dcb997d6acd5	2026-01-23	Warnings	Exact identifier application number: M003
BZK Pads	BENZALKONIUM CHLORIDE	Dynarex Corporation	10454042-ff2e-44ce-b2e2-436cc004897f	2026-01-23	Warnings	Exact identifier application number: M003
Everlit Survival Sting Relief Pad	ISOPROPYL ALCOHOL	EVERLIT GLOBAL INC.	3a0414ea-f862-aa0f-e063-6294a90aecb7	2026-01-23	Warnings	Exact identifier application number: M003
Medline	POVIDONE-IODINE	Medline Industries, LP	48ebfdd6-d346-7e26-e063-6394a90af11a	2026-01-23	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