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NDC 71889-350, TITANIUM DIOXIDE, ZINC OXIDE, cream, from Kapa'ihi, Inc.
- Product NDC
- 71889-350
- Status
- Listed
- Labeler
- Kapa'ihi, Inc
- Dosage form
- CREAM
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M020
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71889-350 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TITANIUM DIOXIDE60 mg/mL
- ZINC OXIDE60 mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71889-350-08 | 71889035008 | 1 BOTTLE in 1 CARTON (71889-350-08) / 236 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 71889-350 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71889-350 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71889-350. 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.