Dryness Relief

Product NDC
17312-178
11-digit product format
173120178
Labeler code
17312
Product ID
17312-178_e71734e0-1bb8-c66e-e053-2995a90a7b9f
Type
HUMAN OTC DRUG
Nonproprietary name
SILVER, SODIUM CHLORIDE, NUTMEG, RUTA GRAVEOLENS, SULFUR, ZINC
Dosage form
LIQUID
Route
OPHTHALMIC
Labeler
TRP Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2021-01-11
Marketing end
0000-00-00
Substance
NUTMEG; RUTA GRAVEOLENS FLOWERING TOP; SILVER; SODIUM CHLORIDE; SULFUR; ZINC
Active strength
12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17312-178DRYNESS RELIEF (SILVER, SODIUM CHLORIDE, NUTMEG, RUTA GRAVEOLENS, SULFUR, ZINC) LIQUID [TRP COMPANY]5Legacy NDC20230211_c54c9cf3-34ab-4dbf-e053-2995a90ad044.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17312-178-15173120178151 BOTTLE, DROPPER in 1 PACKAGE (17312-178-15) > 10 mL in 1 BOTTLE, DROPPER2021-01-110000-00-00NoNoCurrent