Home NDC 69662-111-01 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.
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 70 of 114 · 2,270 matching rows.
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