Home NDC 64616-118-02 RadDefense1
Product NDC 64616-118
Requested package NDC 64616-118-02
11-digit product format 646160118
Labeler code 64616
Product ID 64616-118_462f6a47-7119-f39f-e063-6394a90a2042
Type HUMAN OTC DRUG
Nonproprietary name RadDefense1
Dosage form LIQUID
Route ORAL
Labeler Vitality Works, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-03-02
Substance URANYL NITRATE HEXAHYDRATE; STRYCHNOS NUX-VOMICA SEED; VISCUM ALBUM WHOLE
Active strength 30; 30; 30 [hp_C]/29.6mL; [hp_C]/29.6mL; [hp_C]/29.6mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
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 RadDefense1
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength URANYL NITRATE HEXAHYDRATE 30 [hp_C]/29.6mL STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/29.6mL VISCUM ALBUM WHOLE 30 [hp_C]/29.6mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3V057702FY Internal UNII lookup 269XH13919 Internal UNII lookup E6839Q6DO1 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 64616-118-01 RadDefense1 29.6 mL in 1 BOTTLE, DROPPER LIQUID 29.6 7 64616-118-02 RadDefense1 1 in 1 CARTON LIQUID 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64616-118 RADDEFENSE1 LIQUID [VITALITY WORKS, INC.] 6 Current NDC, Legacy NDC, 2 package rows 20241212_2d7ea007-ef23-4b16-e054-00144ff8d46c.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 64616-118-02 64616011802 1 BOTTLE, DROPPER in 1 CARTON (64616-118-02) / 29.6 mL in 1 BOTTLE, DROPPER (64616-118-01) 2016-03-02 0000-00-00 No No Current