Home NDC 81750-020 Kinfield Relief Balm Anti-Itch Remedy
Product NDC 81750-020
11-digit product format 817500020
Labeler code 81750
Product ID 81750-020_472bacf4-c61c-8f20-e063-6294a90a360b
Type HUMAN OTC DRUG
Nonproprietary name Kinfield Relief Balm Anti-Itch Remedy
Dosage form LOTION
Route TOPICAL
Labeler Kinfield, Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-04-05
Substance OATMEAL
Active strength 10 g/17g
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 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 81750-020-17 ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 81750-020-40 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 81750-020-17 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 81750-020-40 367a005e9d99…383a685ebd0f…
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 Kinfield Relief Balm Anti-Itch Remedy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OATMEAL 10 g/17g
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 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 81750-020-17 Kinfield Relief Balm Anti-Itch Remedy 1 in 1 PACKAGE LOTION 1 6 81750-020-17 Kinfield Relief Balm Anti-Itch Remedy 17 g in 1 TUBE LOTION 17 6 81750-020-40 Kinfield Relief Balm Anti-Itch Remedy 1 in 1 PACKAGE LOTION 1 6 81750-020-40 Kinfield Relief Balm Anti-Itch Remedy 40 g in 1 TUBE LOTION 40 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81750-020 KINFIELD RELIEF BALM ANTI-ITCH REMEDY LOTION [KINFIELD, INC.] 5 Current NDC, Legacy NDC, 4 package rows 20241220_bf394192-c789-faff-e053-2995a90a52bc.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81750-020-17 81750002017 1 TUBE in 1 PACKAGE (81750-020-17) / 17 g in 1 TUBE 1 tube 2021-04-05 0000-00-00 No No Current 81750-020-40 81750002040 1 TUBE in 1 PACKAGE (81750-020-40) / 40 g in 1 TUBE 1 tube 2021-04-05 No No Current