Wet Eczema Drops
- Product NDC
- 63083-2136
- 11-digit product format
- 630832136
- Labeler code
- 63083
- Product ID
- 63083-2136_0597f5dc-11b0-423c-b516-3fea39591f30
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Wet Eczema Drops
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- ARSENIC TRIIODIDE; ARSENIC TRIOXIDE; CALCIUM SULFIDE; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; GRAPHITE; LIQUID PETROLEUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM SULFATE; SULFUR; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 6; 9; 6; 6; 6; 12; 6; 6; 6; 8; 6 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Wet Eczema Drops
- Brand name suffix
- 2136
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARSENIC TRIIODIDE | 6 [hp_X]/59mL |
| ARSENIC TRIOXIDE | 9 [hp_X]/59mL |
| CALCIUM SULFIDE | 6 [hp_X]/59mL |
| CLEMATIS RECTA FLOWERING TOP | 6 [hp_X]/59mL |
| DAPHNE MEZEREUM BARK | 6 [hp_X]/59mL |
| GRAPHITE | 12 [hp_X]/59mL |
| LIQUID PETROLEUM | 6 [hp_X]/59mL |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 6 [hp_X]/59mL |
| POTASSIUM SULFATE | 6 [hp_X]/59mL |
| SULFUR | 8 [hp_X]/59mL |
| TOXICODENDRON PUBESCENS LEAF | 6 [hp_X]/59mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3029988O2T, S7V92P67HO, 1MBW07J51Q, 396421SP9F, X2N6E405GV, 4QQN74LH4O, 6ZAE7X688J, 2E32821G6I, 1K573LC5TV, 70FD1KFU70, 6IO182RP7A |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63083-2136-2 | Wet Eczema Drops2136 | 59 mL in 1 BOTTLE, DROPPER | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-2136 | WET ECZEMA DROPS 2136 (WET ECZEMA DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220216_28f08a29-9b1a-4579-a56f-4cab7cdcfcb6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-2136-2 | 63083213602 | 59 mL in 1 BOTTLE, DROPPER (63083-2136-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |