Vitafol One
NDC 0642-0070, Prenatal Supplement with DHA, capsule, gelatin coated, from Exeltis USA, Inc..
- Product NDC
- 0642-0070
- Status
- Listed
- Labeler
- Exeltis USA, Inc.
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0642-0070 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VITAMIN A330 ug/1
- ASCORBIC ACID30 mg/1
- THIAMINE MONONITRATE1.6 mg/1
- RIBOFLAVIN1.8 mg/1
- NIACIN15 mg/1
- PYRIDOXINE HYDROCHLORIDE2.5 mg/1
- CYANOCOBALAMIN.012 mg/1
- FOLIC ACID1700 ug/1
- IODINE.15 mg/1
- MAGNESIUM20 mg/1
- ZINC25 mg/1
- COPPER2 mg/1
- VITAMIN D25 ug/1
- OMEGA-3 FATTY ACIDS200 mg/1
- .ALPHA.-TOCOPHEROL9 mg/1
- IRON29 mg/1
Pharmacologic classes
Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Fatty Acids, Omega-3 [CS]; Inhibit Ovum Fertilization [PE]; Nicotinic Acid [EPC]; Nicotinic Acids [CS]; Omega-3 Fatty Acid [EPC]; Vitamin A [CS]; Vitamin A [EPC]; Vitamin B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0642-0070-03 | 00642007003 | 1 BLISTER PACK in 1 BOX (0642-0070-03) / 3 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| 0642-0070-30 | 00642007030 | 5 BLISTER PACK in 1 BOX (0642-0070-30) / 6 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/42a5cafd-a2c0-4ac2-99c9-708642f00716NADAC price for package 00642007030
GET /v1/drugs/nadac/00642007030
Use it
Look up 0642-0070 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0642-0070 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0642-0070. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.