Dryness Relief PF
- Product NDC
- 17312-096
- 11-digit product format
- 173120096
- Labeler code
- 17312
- Product ID
- 17312-096_e5d49d8e-26da-ecde-e053-2995a90adc5d
- 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
- 2022-08-09
- 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| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17312-096 | DRYNESS RELIEF PF (SILVER, SODIUM CHLORIDE, NUTMEG, RUTA GRAVEOLENS, SULFUR, ZINC) LIQUID [TRP COMPANY] | 4 | Legacy NDC | 20230223_e5d491e0-b5e0-704c-e053-2995a90af9dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17312-096-19 | 17312009619 | 1 BOTTLE, DROPPER in 1 PACKAGE (17312-096-19) > 10 mL in 1 BOTTLE, DROPPER | 2022-08-09 | 0000-00-00 | No | No | Current |