DNA Insulin Drops

Product NDC
63083-2019
Requested package NDC
63083-2019-2
11-digit product format
630832019
Labeler code
63083
Product ID
63083-2019_91ade3ff-25ab-464b-8084-9fb5d5d6d955
Type
HUMAN OTC DRUG
Nonproprietary name
DNA Insulin Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
CHROMIUM; INSULIN GLULISINE; LYCOPODIUM CLAVATUM SPORE; PANCRELIPASE AMYLASE; PHOSPHORIC ACID; RADIUM BROMIDE; URANYL NITRATE HEXAHYDRATE; VANADIUM
Active strength
6; 12; 6; 6; 30; 60; 30; 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Insulin Analog [EPC], Insulin [Chemical/Ingredient], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
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 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

Additional Listing Data#

Finished product
Yes
Brand name base
DNA Insulin Drops
Brand name suffix
2019
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CHROMIUM6 [hp_X]/59mL
LYCOPODIUM CLAVATUM SPORE12 [hp_X]/59mL
VANADIUM6 [hp_X]/59mL
PANCRELIPASE AMYLASE6 [hp_X]/59mL
INSULIN GLULISINE30 [hp_X]/59mL
PHOSPHORIC ACID60 [hp_X]/59mL
URANYL NITRATE HEXAHYDRATE30 [hp_X]/59mL
RADIUM BROMIDE6 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0R0008Q3JBInternal UNII lookup
C88X29Y479Internal UNII lookup
00J9J9XKDEInternal UNII lookup
YOJ58O116EInternal UNII lookup
7XIY785AZDInternal UNII lookup
E4GA8884NNInternal UNII lookup
3V057702FYInternal UNII lookup
R74O7T8569Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
527dbb62-5c68-4ea8-93c7-48122817d6a5Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b1603b8-969e-b082-f6f5-ad66d8a6ea8aProduct name220200325
19041f15-771b-3d3a-88fc-f5e2d079cd6dProduct name220200325
1987d950-08e4-4b70-adeb-fb67a71142abProduct name220200325
8825ddf7-1520-4680-b0ee-684e2fa73672Product name220200325
267a6f34-90b4-2f48-3063-4f505d06a7beProduct name120140508

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-09C19
2026-01-09C19
2024-01-30C19
2024-01-30C19

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2019-2DNA Insulin Drops201959 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2019DNA INSULIN DROPS 2019 (DNA INSULIN DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220215_527dbb62-5c68-4ea8-93c7-48122817d6a5.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DNA Insulin Drops 2019DNA INSULIN DROPSProfessional Complementary Health Formulas527dbb62-5c68-4ea8-93c7-48122817d6a52026-01-08WarningsExact identifier
ndc (package): 63083-2019-2
ndc (product): 63083-2019
ndc11 (package): 63083201902

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2019-26308320190259 mL in 1 BOTTLE, DROPPER (63083-2019-2) 59 ml1985-08-150000-00-00NoNoCurrent