Home NDC 76420-766-01 DoubleDex Kit
Product NDC 76420-766
Requested package NDC 76420-766-01
11-digit product format 764200766
Labeler code 76420
Product ID 76420-766_47db098f-6da3-2339-e063-6294a90a4c84
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Dexamethasone Sodium Phosphate, Povidine Iodine
Dosage form KIT
Route INTRAMUSCULAR; INTRAVENOUS; TOPICAL
Labeler Asclemed USA, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2014-07-25
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 DoubleDex Kit
Listing expiration 2027-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 797544 Internal RxNorm lookup 797730 Internal RxNorm lookup 1812079 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 76420-766-01 DoubleDex Kit 1 in 1 CARTON KIT 1 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Dexamethasone Sodium Phosphate ACTIVE INGREDIENT AI9376Y64P DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Isopropyl Alcohol ACTIVE INGREDIENT ND2M416302 DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Povidone-Iodine ACTIVE INGREDIENT 85H0HZU99M DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Dexamethasone ACTIVE MOIETY 7S5I7G3JQL DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Iodine ACTIVE MOIETY 9679TC07X4 DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Isopropyl Alcohol ACTIVE MOIETY ND2M416302 DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Citric Acid Monohydrate INACTIVE INGREDIENT 2968PHW8QP DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Nonoxynol-9 INACTIVE INGREDIENT 48Q180SH9T DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Sodium Citrate INACTIVE INGREDIENT 1Q73Q2JULR DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Sodium Hydroxide INACTIVE INGREDIENT 55X04QC32I DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1 Water INACTIVE INGREDIENT 059QF0KO0R DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76420-766 DOUBLEDEX KIT (DEXAMETHASONE SODIUM PHOSPHATE, POVIDINE IODINE) KIT [ASCLEMED USA, INC.] 8 Current NDC, Legacy NDC, 1 package rows 20241008_b7d58d9b-e1fa-4a7f-afca-beb06d028057.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 1 · 1 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 76420-766-01 76420076601 1 KIT in 1 CARTON (76420-766-01) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL 1 kit 2016-05-23 0000-00-00 No No Current