Home NDC 10237-858 ARRID EXTRA EXTRA DRY XX
Product NDC 10237-858
11-digit product format 102370858
Labeler code 10237
Product ID 10237-858_37533b37-3bcc-36f7-e063-6394a90a8b19
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Church & Dwight Co., Inc.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-04-22
Substance ALUMINUM CHLOROHYDRATE
Active strength 246 mg/g
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.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Additional Listing Data#
Finished product Yes
Brand name base ARRID EXTRA EXTRA DRY XX
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 246 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HPN8MZW13M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10237-858-40 ARRID EXTRA EXTRA DRY XX 113 g in 1 CAN AEROSOL, SPRAY 113 6 10237-858-60 ARRID EXTRA EXTRA DRY XX 170 g in 1 CAN AEROSOL, SPRAY 170 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALUMINUM CHLOROHYDRATE ACTIVE INGREDIENT HPN8MZW13M ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 ALUMINUM CATION ACTIVE MOIETY 3XHB1D032B ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 1,1-DIFLUOROETHANE INACTIVE INGREDIENT 0B1U8K2ME0 ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 BUTANE INACTIVE INGREDIENT 6LV4FOR43R ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 CYCLOMETHICONE 5 INACTIVE INGREDIENT 0THT5PCI0R ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 HECTORITE INACTIVE INGREDIENT 08X4KI73EZ ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1 PROPYLENE CARBONATE INACTIVE INGREDIENT 8D08K3S51E ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10237-858 ARRID EXTRA EXTRA DRY XX (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CHURCH & DWIGHT CO., INC.] 5 Current NDC, Legacy NDC, 2 package rows 20241120_2c36567e-fe89-4418-8ce8-87bcc05375d8.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 1 of 74 · 1,465 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10237-858-40 10237085840 113 g in 1 CAN (10237-858-40) 113 g 2011-04-22 0000-00-00 No No Current 10237-858-60 10237085860 170 g in 1 CAN (10237-858-60) 170 g 2011-04-22 2022-12-31 No No Current