Home NDC 67234-010 Natureplex Hydrocortisone
Product NDC 67234-010
11-digit product format 672340010
Labeler code 67234
Product ID 67234-010_c04d26f2-8870-4d41-91a9-519c349b517a
Type HUMAN OTC DRUG
Nonproprietary name Hydrocortisone
Dosage form CREAM
Route TOPICAL
Labeler Natureplex, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-01-22
Substance HYDROCORTISONE
Active strength .01 g/g
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 Natureplex Hydrocortisone
Brand name suffix Hydro
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYDROCORTISONE .01 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WI4X0X7BPJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 106258 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 67234-010-01 Natureplex HydrocortisoneHydro 28 g in 1 TUBE CREAM 28 16 67234-010-02 Natureplex HydrocortisoneHydro 42.5 g in 1 TUBE CREAM 42.5 16 67234-010-02 Natureplex HydrocortisoneHydro 1 in 1 CARTON CREAM 1 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Hydrocortisone ACTIVE INGREDIENT WI4X0X7BPJ NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 Hydrocortisone ACTIVE MOIETY WI4X0X7BPJ NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 alcohol INACTIVE INGREDIENT 3K9958V90M NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 Aloe Vera Leaf INACTIVE INGREDIENT ZY81Z83H0X NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 carbomer homopolymer type C INACTIVE INGREDIENT 4Q93RCW27E NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 cetyl alcohol INACTIVE INGREDIENT 936JST6JCN NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 DMDM Hydantoin INACTIVE INGREDIENT BYR0546TOW NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 edetate trisodium INACTIVE INGREDIENT 420IP921MB NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 glyceryl monostearate INACTIVE INGREDIENT 230OU9XXE4 NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 methylparaben INACTIVE INGREDIENT A2I8C7HI9T NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 mineral oil INACTIVE INGREDIENT T5L8T28FGP NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 polysorbate 20 INACTIVE INGREDIENT 7T1F30V5YH NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 propylparaben INACTIVE INGREDIENT Z8IX2SC1OH NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 stearic acid INACTIVE INGREDIENT 4ELV7Z65AP NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 trolamine INACTIVE INGREDIENT 9O3K93S3TK NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12 water INACTIVE INGREDIENT 059QF0KO0R NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67234-010 NATUREPLEX HYDROCORTISONE HYDRO (HYDROCORTISONE) CREAM [NATUREPLEX, LLC] 14 Current NDC, Legacy NDC, 3 package rows 20250101_2fc6a148-34bb-4289-8588-32c1bb011b98.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 44 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lidocaine HCI LIDOCAINE HCI Trifluent Pharma, LLC 47f7f06b-720e-eeec-e063-6294a90ae823 2026-01-09 Warnings Exact identifier application number: M017 Lidocaine LIDOCAINE Bellus Medical, LLC 60cb89f6-e326-0773-e053-2a91aa0a33dd 2026-01-09 Warnings Exact identifier application number: M017 Tetracaine TETRACAINE Bellus Medical, LLC 60cabb5f-606b-7a74-e053-2a91aa0ac024 2026-01-09 Warnings Exact identifier application number: M017 Benzocaine BENZOCAINE Bellus Medical, LLC 60cafbaf-8ec6-46a5-e053-2a91aa0af11f 2026-01-09 Warnings Exact identifier application number: M017 PRAX PRAMOXINE HYDROCHLORIDE AvPAK dc646399-91ba-5cc1-e053-2a95a90a4f9c 2026-01-09 Warnings Exact identifier application number: M017 2.5% Menthol PAIN RELIEF MENTHOL Universal Distribution Center LLC c842544a-6aea-42af-a77e-7b202371b387 2026-01-09 Warnings Exact identifier application number: M017 4% Menthol PAIN RELIEF MENTHOL Universal Distribution Center LLC 7fb95135-4151-4ef4-bb6d-75251cafff6c 2026-01-09 Warnings Exact identifier application number: M017 Meijer Extra Strength Cold And Hot TherapyPain Relieving Topical Analgesic MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE Meijer Distribution, Inc 781f89c0-94ab-48de-9e0b-decb37bcde46 2026-01-09 Warnings Exact identifier application number: M017 LIDOCAINE PAIN RELIEVING Gel-Patch LIDOCAINE Guangzhou Zhupuyou E-commerce Co., Ltd 2159fb73-cf6c-184a-e063-6394a90a1d14 2026-01-08 Warnings Exact identifier application number: M017 PAIN RELIEF Gel-Patch LIDOCAINE, MENTHOL Guangzhou Zhupuyou E-commerce Co., Ltd 22d9ce20-1cb6-c5bd-e063-6394a90a9eca 2026-01-08 Warnings Exact identifier application number: M017 AY BENDITO - THERMOACTIVE CAMPHOR, MENTHOL AY BENDITO INT'L THERMO ANALGETICS ROLL-ON 76ef713b-e23d-7b98-e053-2991aa0aad51 2026-01-08 Warnings Exact identifier application number: M017 AY BENDITO - THERMOACTIVE CAMPHOR, MENTHOL AY BENDITO INTERNATIONAL, INC bbf0ca84-2800-d222-e053-2995a90ad8f3 2026-01-08 Warnings Exact identifier application number: M017 Capsaicin CAPSAICIN AvPAK ef5b0db6-8f0a-4f8e-e053-2995a90a22b7 2026-01-08 Warnings Exact identifier application number: M017 Capsaicin Topical Analgesic CAPSAICIN AvPAK ef597423-cd01-7324-e053-2a95a90aa1ba 2026-01-08 Warnings Exact identifier application number: M017 Capsaicin External Analgesic CAPSAICIN AvPAK ef5a3846-1d2f-7023-e053-2a95a90ad716 2026-01-08 Warnings Exact identifier application number: M017 Capsaicin CAPSAICIN AvPAK ef5bb0fa-afc2-62d7-e053-2a95a90a37f4 2026-01-08 Warnings Exact identifier application number: M017 K2 Cold Therapy MENTHOL The Podiatree Co 60dce1ad-125e-396d-e053-2a91aa0a670f 2026-01-08 Warnings Exact identifier application number: M017 Burn Relief Aloe LIDOCAINE HCL Acutens 48c435fe-2670-4b80-bf01-923dc9354422 2026-01-08 Warnings Exact identifier application number: M017 Relieve A Pain LIDOCAINE Relieve A Pain LLC cafaa830-d894-4590-8928-d579cc791d79 2026-01-08 Warnings Exact identifier application number: M017 DZUL ARTHRITIS PAIN RELIEF MENTHOL Caball Sales, Inc. 159c301c-d462-bb2c-e063-6394a90a9e5a 2026-01-08 Warnings Exact identifier application number: M017
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 67234-010-01 67234001001 28 g in 1 TUBE (67234-010-01) 28 g 2008-01-22 0000-00-00 No No Current 67234-010-02 67234001002 1 TUBE in 1 CARTON (67234-010-02) / 42.5 g in 1 TUBE 1 tube 2022-12-09 No No Current