Home NDC 71753-8012 Silicea
Product NDC 71753-8012
11-digit product format 717538012
Labeler code 71753
Product ID 71753-8012_7e565ef2-5239-46c1-854c-4aaf63683a7f
Type HUMAN OTC DRUG
Nonproprietary name Silicea
Dosage form SPRAY
Route ORAL
Labeler Ratis, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-09-30
Substance SILICON DIOXIDE
Active strength 12 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Silicea
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILICON DIOXIDE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ETJ7Z6XBU4 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71753-8012-1 Silicea 30 mL in 1 BOTTLE, SPRAY SPRAY 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71753-8012 SILICEA SPRAY [RATIS, LLC] 4 Current NDC, Legacy NDC, 1 package rows 20230714_8c2b59e1-9936-486c-9a91-153e46f377e6.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71753-8012-1 71753801201 30 mL in 1 BOTTLE, SPRAY (71753-8012-1) 30 ml 2020-09-30 0000-00-00 No No Current