Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Asthma Drops 2010 (asthma drops) NDC 63083-2010
Aralia racemosa root 3 [hp_X]/59mL + 14 more ingredients · Liquid · Oral · Professional Complementary Health Formulas
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63083-2010-2 | 63083201002 | 59 mL in 1 BOTTLE, DROPPER (63083-2010-2)Marketed from Aug 15, 1985 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Asthma Drops 2010Suffix: 2010
- Generic name (nonproprietary)
- asthma drops
- Active ingredients
- Aralia racemosa root — 3 [hp_X]/59mLLobelia cardinalis whole — 3 [hp_X]/59mLSpongia officinalis skeleton, Roasted — 3 [hp_X]/59mLAntimony potassium tartrate — 8 [hp_X]/59mLAconitum napellus whole — 6 [hp_X]/59mLSus scrofa adrenal gland — 6 [hp_X]/59mLBlatta orientalis — 6 [hp_X]/59mLCopper — 6 [hp_X]/59mLIodine — 6 [hp_X]/59mLIpecac — 6 [hp_X]/59mLLobelia inflata whole — 6 [hp_X]/59mLBeef lung — 6 [hp_X]/59mLArsenic trioxide — 12 [hp_X]/59mLSulfur — 12 [hp_X]/59mLOyster shell calcium carbonate, Crude — 30 [hp_X]/59mL
- Dosage form
- Liquid
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Insect Proteins (Chemical structure)
- Identifiers
- Product ID 63083-2010_8de781b3-de2f-4edb-89ca-6640ab72c1faSPL ID 8de781b3-de2f-4edb-89ca-6640ab72c1faSPL set ID b9f234ad-a5ff-40a9-bc51-c192f3014090UNII T90W4582DU, GT0PJ8MB5R, 1PIP394IID, DL6OZ476V3, U0NQ8555JD, 398IYQ16YV, 535787266D, 789U1901C5, 9679TC07X4, 62I3C8233L, 9PP1T3TC5U, 2I1RTO1MBR, S7V92P67HO, 70FD1KFU70, 2E32821G6I
- Pharmacologic class
- Copper-containing Intrauterine Device; Non-Standardized Insect Allergenic Extract
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N463083201002followed by a unit qualifier and the quantityPackage 63083-2010-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS For the temporary relief of wheezing, coughing, chest tightness or shortness of breath due to aerobic exercise, obesity, anxiousness, smoking, or exposure to pollutants, allergens, or environmental toxins.*
Excerpt only. Read the full label for complete information.