Home NDC 0363-0619 Daily Moisturizing
Product NDC 0363-0619
11-digit product format 003630619
Labeler code 0363
Product ID 0363-0619_4ce9e80c-6931-41fb-e063-6394a90a1cb1
Type HUMAN OTC DRUG
Nonproprietary name Daily Moistruizing
Dosage form LOTION
Route TOPICAL
Labeler Walgreen Co.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-02-06
Substance DIMETHICONE
Active strength 13 mg/g
Pharmacologic classes Skin Barrier Activity [PE]
NDC exclude flag No
Listing certified through 2027-12-31
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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0363-0619 0363-0619-44 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0363-0619 0363-0619-44 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
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 Daily Moisturizing
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE 13 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 891710 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-0619-18 Daily Moisturizing 71 g in 1 TUBE LOTION 71 20 0363-0619-34 Daily Moisturizing 227 g in 1 TUBE LOTION 227 20 0363-0619-44 Daily Moisturizing 532 g in 1 BOTTLE, PLASTIC LOTION 532 20
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-0619 DAILY MOISTURIZING (DAILY MOISTRUIZING) LOTION [WALGREEN, CO.] 18 Current NDC, Legacy NDC, 3 package rows 20250409_27452cc7-1ec6-4571-bcd0-0a7103735ee5.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 39 of 68 · 1,350 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 0363-0619-18 00363061918 71 g in 1 TUBE (0363-0619-18) 71 g 2013-02-06 0000-00-00 No No Current 0363-0619-34 00363061934 227 g in 1 TUBE (0363-0619-34) 227 g 2013-02-06 0000-00-00 No No Current 0363-0619-44 00363061944 532 g in 1 BOTTLE, PLASTIC (0363-0619-44) 532 g 2013-02-06 0000-00-00 No No Current