FDA.reportPublic FDA data

FRESH AQUA

Product NDC
70610-105
11-digit product format
706100105
Labeler code
70610
Product ID
70610-105_738089fd-716b-237e-e053-2991aa0a1a99
Type
HUMAN OTC DRUG
Nonproprietary name
Trisodium Phosphate
Dosage form
LIQUID
Route
TOPICAL
Labeler
KOTUKU INC.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-08-13
Marketing end
0000-00-00
Substance
SODIUM PHOSPHATE, TRIBASIC, DODECAHYDRATE
Active strength
1 g/475mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70610-105-012020-01-31C16284748780-19d75b9d0-62b0-f424-e053-dadaa90a57ceFRESH AQUA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70610-105-01FRESH AQUA475 mL in 1 BOTTLE, SPRAYLIQUID4751

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70610-105FRESH AQUA (TRISODIUM PHOSPHATE) LIQUID [KOTUKU INC.]1Legacy NDC, 1 package rows20180816_738089fd-716a-237e-e053-2991aa0a1a99.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70610-105-0170610010501475 mL in 1 BOTTLE, SPRAY475 mlHistorical