NDC product
Dr. Talbots Tummy Ache Relief
NDC 70797-311 · Talbot's Pharmaceuticals Family Products, LLC
Key facts
| Product NDC | 70797-311 |
|---|---|
| Proprietary name | Dr. Talbots Tummy Ache Relief |
| Nonproprietary name | Calendula officinalis, Carbo vegetabilis, Chamomilla, Foeniculum vulgare, Lycopodium, Nux moschata, Zingiber officinale, Kali muriaticum, Magnesia phosphorica, Natrum phosphoricum |
| Substances | ACTIVATED CHARCOAL, NUTMEG, POTASSIUM CHLORIDE, MATRICARIA CHAMOMILLA, CALENDULA OFFICINALIS FLOWERING TOP, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, LYCOPODIUM CLAVATUM SPORE, GINGER, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, FENNEL SEED |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Talbot's Pharmaceuticals Family Products, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE] and 13 more |
| Marketing start | Jul 10, 2020 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: