Naturasil

Product NDC
10893-110
11-digit product format
108930110
Labeler code
10893
Product ID
10893-110_6a6e3055-223d-428b-a812-d87d50cd461c
Type
HUMAN OTC DRUG
Nonproprietary name
Phosphoricum Acidum
Dosage form
LIQUID
Route
TOPICAL
Labeler
Nature's Innovation, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-01-13
Substance
PHOSPHORIC ACID
Active strength
6 [hp_X]/10mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Naturasil
Brand name suffix
Bite Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHOSPHORIC ACID6 [hp_X]/10mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiE4GA8884NN

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10893-110-10NaturasilBite Relief10 mL in 1 BOTTLE, GLASSLIQUID104

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10893-110NATURASIL BITE RELIEF (PHOSPHORICUM ACIDUM) LIQUID [NATURE'S INNOVATION, INC.]4Current NDC, Legacy NDC, 1 package rows20210115_4a355788-ea13-4323-a55c-d3b1dab8251e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10893-110-101089301101010 mL in 1 BOTTLE, GLASS (10893-110-10) 10 ml2012-01-130000-00-00NoNoCurrent