K-OK Kiddie Calmer

Product NDC
68703-049
11-digit product format
687030049
Labeler code
68703
Product ID
68703-049_838468cd-25e2-4df4-abc4-ddc572984215
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitinum, silicea
Dosage form
GRANULE
Route
ORAL
Labeler
Native Remedies, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-08-01
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS; SILICON DIOXIDE
Active strength
6 [hp_C]/100mg; [hp_C]/100mg
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68703-049-202020-01-31C16284748780-19d75b9d0-13f3-f424-e053-dadaa90a57ceK-OK Kiddie Calmer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68703-049-20K-OK Kiddie Calmer20000 mg in 1 BOTTLE, GLASSGRANULE200001

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68703-049K-OK KIDDIE CALMER (ACONITINUM, SILICEA) GRANULE [NATIVE REMEDIES, LLC]1Legacy NDC, 1 package rows20120906_d407b134-0605-4641-929c-f2eae046ca02.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
68703-049-206870300492020000 mg in 1 BOTTLE, GLASS20000 mgHistorical