Nocturnal Enuresis Drops

Product NDC
63083-2011
Requested package NDC
63083-2011-2
11-digit product format
630832011
Labeler code
63083
Product ID
63083-2011_c58ac174-b51a-4fa1-a4cf-1325ec9abf90
Type
HUMAN OTC DRUG
Nonproprietary name
Nocturnal Enuresis Drops
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Substance
SUS SCROFA URINARY BLADDER; THYROID, UNSPECIFIED; CAUSTICUM; EQUISETUM HYEMALE WHOLE; FERROSOFERRIC PHOSPHATE; WOOD CREOSOTE; PULSATILLA MONTANA WHOLE; ANHYDROUS DIBASIC CALCIUM PHOSPHATE
Active strength
6; 6; 12; 12; 12; 12; 12; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
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…

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
Nocturnal Enuresis Drops
Brand name suffix
2011
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUS SCROFA URINARY BLADDER6 [hp_X]/59mL
THYROID, UNSPECIFIED6 [hp_X]/59mL
CAUSTICUM12 [hp_X]/59mL
EQUISETUM HYEMALE WHOLE12 [hp_X]/59mL
FERROSOFERRIC PHOSPHATE12 [hp_X]/59mL
WOOD CREOSOTE12 [hp_X]/59mL
PULSATILLA MONTANA WHOLE12 [hp_X]/59mL
ANHYDROUS DIBASIC CALCIUM PHOSPHATE12 [hp_X]/59mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 8 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3G7U72W8DAInternal UNII lookup
0B4FDL9I6PInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
59677RXH25Internal UNII lookup
91GQH8I5F7Internal UNII lookup
3JYG22FD73Internal UNII lookup
24K790T39BInternal UNII lookup
L11K75P92JInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
9cd29086-c9eb-4db1-a219-2a8bae3663d8Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2026-01-09C11
2026-01-09C11
2024-01-30C11
2024-01-30C11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2011-2Nocturnal Enuresis Drops201159 mL in 1 BOTTLE, DROPPERLIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-2011NOCTURNAL ENURESIS DROPS 2011 (NOCTURNAL ENURESIS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Current NDC, Legacy NDC, 1 package rows20220216_9cd29086-c9eb-4db1-a219-2a8bae3663d8.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
Nocturnal Enuresis Drops 2011NOCTURNAL ENURESIS DROPSProfessional Complementary Health Formulas9cd29086-c9eb-4db1-a219-2a8bae3663d82026-01-08WarningsExact identifier
ndc (package): 63083-2011-2
ndc (product): 63083-2011
ndc11 (package): 63083201102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-2011-26308320110259 mL in 1 BOTTLE, DROPPER (63083-2011-2) 59 ml1985-08-150000-00-00NoNoCurrent