ANXIETY II HP
- Product NDC
- 43406-0004
- 11-digit product format
- 434060004
- Labeler code
- 43406
- Product ID
- 43406-0004_b274cc51-dd50-430a-bc9e-ad8c1b6be455
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Arsenic Trioxide, Atropa Belladonna, Oyster Shell Calcium Carbonate, Crude, Activated Charcoal, Human Breast Tumor Cell, Causticum, Gelsemium Sempervirens Root, Lachesis Muta Venom, Mercury, Sodium Chloride, Nitric Acid, Phosphorus, Toxicodendron Pubescens Leaf
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2007-05-29
- Substance
- ACONITUM NAPELLUS WHOLE; ACTIVATED CHARCOAL; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CAUSTICUM; GELSEMIUM SEMPERVIRENS ROOT; HUMAN BREAST TUMOR CELL; LACHESIS MUTA VENOM; MERCURY; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANXIETY II HP
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS WHOLE | 30 [hp_C]/mL |
| ACTIVATED CHARCOAL | 30 [hp_C]/mL |
| ARSENIC TRIOXIDE | 30 [hp_C]/mL |
| ATROPA BELLADONNA | 30 [hp_C]/mL |
| CAUSTICUM | 30 [hp_C]/mL |
| GELSEMIUM SEMPERVIRENS ROOT | 30 [hp_C]/mL |
| HUMAN BREAST TUMOR CELL | 30 [hp_C]/mL |
| LACHESIS MUTA VENOM | 30 [hp_C]/mL |
| MERCURY | 30 [hp_C]/mL |
| NITRIC ACID | 30 [hp_C]/mL |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 30 [hp_C]/mL |
| PHOSPHORUS | 30 [hp_C]/mL |
| SODIUM CHLORIDE | 30 [hp_C]/mL |
| TOXICODENDRON PUBESCENS LEAF | 30 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U0NQ8555JD, 2P3VWU3H10, S7V92P67HO, WQZ3G9PF0H, DD5FO1WKFU, 639KR60Q1Q, C62OO7VD9K, VSW71SS07I, FXS1BY2PGL, 411VRN1TV4, 2E32821G6I, 27YLU75U4W, 451W47IQ8X, 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 |
|---|
| 43406-0004-1 | ANXIETY II HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43406-0004 | ANXIETY II HP (ACONITUM NAPELLUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACTIVATED CHARCOAL, HUMAN BREAST TUMOR CELL, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF) LIQUID [NATURAL CREATIONS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20220218_02fa45a5-08e1-41ad-acd4-0f85db07e89e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43406-0004-1 | 43406000401 | 30 mL in 1 BOTTLE, DROPPER (43406-0004-1) | 30 ml | 2007-05-29 | 0000-00-00 | No | No | Current |