Home NDC 64942-1503 Dove
Product NDC 64942-1503
11-digit product format 649421503
Labeler code 64942
Product ID 64942-1503_253be68a-9666-b800-e063-6294a90ad488
Type HUMAN OTC DRUG
Nonproprietary name Colloidal Oatmeal
Dosage form LOTION
Route TOPICAL
Labeler Conopco, Inc. d/b/a/ Unilever
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-07-13
Substance OATMEAL
Active strength 1 g/100mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 · 6 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 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 64942-1503-1 e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 64942-1503-2 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 64942-1503-1 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 64942-1503-2 9bebd1f3094a…5416666fcb17…
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 Dove
Brand name suffix DermaSeries Eczema Relief Soothing Body
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OATMEAL 1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8PI54V663Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 240464 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64942-1503-1 DoveDermaSeries Eczema Relief Soothing Body 50 mL in 1 TUBE LOTION 50 5 64942-1503-2 DoveDermaSeries Eczema Relief Soothing Body 200 mL in 1 TUBE LOTION 200 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64942-1503 DOVE DERMASERIES ECZEMA RELIEF SOOTHING BODY (COLLOIDAL OATMEAL) LOTION [CONOPCO, INC. D/B/A/ UNILEVER] 5 Current NDC, Legacy NDC, 2 package rows 20241027_59f737f6-dd3f-4b63-b13e-2345cb9a951a.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 · 1,357 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 64942-1503-1 64942150301 50 mL in 1 TUBE (64942-1503-1) 50 ml 2017-07-13 0000-00-00 No No Current 64942-1503-2 64942150302 200 mL in 1 TUBE (64942-1503-2) 200 ml 2017-07-13 0000-00-00 No No Current