Home NDC 69662-111 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.
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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 109 of 115 · 2,286 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ethyl Rubbing Alcohol 70 Percent ETHYL ALCOHOL Pharma Nobis, LLC e42fccc2-1b50-e7f3-e053-2a95a90aef39 2023-12-26 Warnings Exact identifier application number: M003 Isopropyl Alcohol 70 Percent With Wintergreen Oil ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f6c6d-c4e1-02c6-e053-2995a90a3ace 2023-12-26 Warnings Exact identifier application number: M003 CVS Merthiolate BENZALKONIUM CHLORIDE CVS Pharmacy dd498ab1-8350-41aa-86fc-2db57005f3e2 2023-12-22 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE IODINE 10% Pharma Nobis, LLC e42eee1b-3539-fb17-e053-2995a90af61d 2023-12-22 Warnings Exact identifier application number: M003 Decolorized Iodine ETHYL ALCOHOL Pharma Nobis, LLC e21dd43b-3712-cb16-e053-2a95a90ac276 2023-12-22 Warnings Exact identifier application number: M003 Isopropyl Rubbing Alcohol 70 Percent ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f727c-beb0-fe9d-e053-2995a90aafea 2023-12-22 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE IODINE GARGLE 0.5% Pharma Nobis, LLC e42ee827-b350-7b56-e053-2a95a90a69cf 2023-12-22 Warnings Exact identifier application number: M003 Merthiolate BENZALKONIUM CHLORIDE Pharma Nobis, LLC e42f727c-beaf-fe9d-e053-2995a90aafea 2023-12-22 Warnings Exact identifier application number: M003 Isopropyl Alcohol 91 Percent ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f6c6d-c4e0-02c6-e053-2995a90a3ace 2023-12-22 Warnings Exact identifier application number: M003 RevitaDERM Wound Care BENZALKONIUM CHLORIDE Blaine Labs Inc. 9254dada-4e32-43a0-892b-c488d68e23e7 2023-12-21 Warnings Exact identifier application number: M003 NUMSTAT Antiseptic and Pain Relieving Prep Pad ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD Spectra Medical Devices, LLC 07d20040-9dd9-0aba-e063-6294a90ab7cf 2023-12-20 Warnings Exact identifier application number: M003 Health Mart Iodides ALCOHOL Strategic Sourcing Services LLC 8d9f2112-c678-4559-b567-9d6d287c5fa3 2023-12-20 Warnings Exact identifier application number: M003 Health Mart Iodine Tincture Mild IODINE AND SODIUM IODIDE AND ALCOHOL Strategic Sourcing Services LLC 72eeb3e6-c0a1-4b18-87f1-8db06f9bd111 2023-12-20 Warnings Exact identifier application number: M003 Health Mart Hydrogen Peroxide 3 Percent HYDROGEN PEROXIDE Strategic Sourcing Services LLC cbe02fa1-c167-4b77-8f63-817362090e19 2023-12-20 Warnings Exact identifier application number: M003 Health Mart Isopropyl Alcohol 91 Percent ISOPROPYL ALCOHOL Strategic Sourcing Services LLC fbd2aa69-b1c7-4a28-9642-a436ae09faaf 2023-12-20 Warnings Exact identifier application number: M003 Quality Choice Povidone Iodine POVIDONE IODINE 10% Chain Drug Market Association 9fa49a3c-ad09-4d35-8cd9-e1a0f2da0d2d 2023-12-20 Warnings Exact identifier application number: M003 Quality Choice Iodine Tincture Mild IODINE AND SODIUM IODIDE AND ALCOHOL Chain Drug Market Association 55c970ed-13a9-4ea2-a8cb-aaf14d3a214d 2023-12-20 Warnings Exact identifier application number: M003 Quality Choice Iodides Tincture ETHYL ALCOHOL Chain Drug Market Association 71aedfd5-e81f-4b69-b163-527ff1ce30b1 2023-12-20 Warnings Exact identifier application number: M003 Quality Choice Merthiolate BENZALKONIUM CHLORIDE Chain Drug Market Association 5b7303b9-b8c4-4e7c-876f-70ed76443055 2023-12-20 Warnings Exact identifier application number: M003 Premier Value Povidone Iodine POVIDONE IODINE 10% Chain Drug Consortium 5cc9d782-5f7e-27d9-e053-2991aa0a2428 2023-12-20 Warnings Exact identifier application number: M003
DailyMed RxNorm Mappings# 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