Anbesol Maximum Strength
NDC 80070-220, BENZOCAINE, gel, from Foundation Consumer Brands.
- Product NDC
- 80070-220
- Status
- Listed
- Labeler
- Foundation Consumer Brands
- Dosage form
- GEL
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M022
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80070-220 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BENZOCAINE200 mg/g
Pharmacologic classes
Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Standardized Chemical Allergen [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80070-220-33 | 80070022033 | 1 TUBE in 1 BLISTER PACK (80070-220-33) / 9 g in 1 TUBE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 80070-220 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80070-220 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80070-220. 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.