Home NDC 52915-010 ECZEMA
Product NDC 52915-010
11-digit product format 529150010
Labeler code 52915
Product ID 52915-010_9bcc07a8-7007-4b41-83e2-d147abb7dbb1
Type HUMAN OTC DRUG
Nonproprietary name OATMEAL
Dosage form LOTION/SHAMPOO
Route TOPICAL
Labeler ORGANIC & SUSTAINABLE BEAUTY
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-10-01
Substance OATMEAL
Active strength 10 mg/mL
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 2020-06-10 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 52915-010-19 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 52915-010-05 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 52915-010-19 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 52915-010-05 110d247fa046…a55b01930146…
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 ECZEMA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OATMEAL 10 mg/mL
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 1437616 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 52915-010-05 ECZEMA 14 mL in 1 TUBE LOTION/SHAMPOO 14 3 52915-010-19 ECZEMA 562 mL in 1 BOTTLE, PUMP LOTION/SHAMPOO 562 3 52915-010-85 ECZEMA 251 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 251 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52915-010 ECZEMA (OATMEAL) LOTION/SHAMPOO [ORGANIC & SUSTAINABLE BEAUTY] 3 Current NDC, Legacy NDC, 3 package rows 20241107_81eb3df4-5beb-45aa-82ca-e8b4b37e45f4.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 52 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 52915-010-05 52915001005 14 mL in 1 TUBE (52915-010-05) 14 ml 2012-10-01 0000-00-00 No No Current 52915-010-19 52915001019 562 mL in 1 BOTTLE, PUMP (52915-010-19) 562 ml 2012-10-01 0000-00-00 No No Current 52915-010-85 52915001085 251 mL in 1 BOTTLE, PLASTIC (52915-010-85) 251 ml 2012-10-01 0000-00-00 No No Current