Labeler
Kapa'ihi, Inc NDC Codes
Kapa'ihi, Inc lists 1 finished drug product in the FDA NDC Directory under NDC labeler code 71889.
Overview
Each product below links to its own NDC page with package NDCs in 10- and 11-digit form.
- Active ingredients
- Titanium dioxide, Zinc oxide
- NDC labeler codes
- 71889
- Strengths
- Titanium dioxide 60 mg/mL; Zinc oxide 60 mg/mL
- Dosage forms
- Cream
- Routes
- Topical
- Drug classes (FDA established)
- Copper Absorption Inhibitor
- HCPCS / J-code
- None in Med-Code's directory for these products
- Package NDCs
- 1
NDC codes
Newest listings first. Each row links to the product’s NDC page.
| Product | Strength | Form · route | Product NDC | Package NDCs (11-digit) | HCPCS |
|---|---|---|---|---|---|
| koa protect our ocean life OXYBENZONE FREE Broad Spectrum SPF 30 UVA UVB Protection Sunscreentitanium dioxide, zinc oxide | Titanium dioxide 60 mg/mL; Zinc oxide 60 mg/mL | CreamTopical | 71889-350 | 71889-0350-08 | — |
Kapa'ihi, Inc: common questions
- What is Kapa'ihi, Inc's NDC labeler code?
- 71889. The labeler code is the first segment of each NDC. About labeler codes.
- Is there a J-code for Kapa'ihi, Inc?
- Med-Code's curated HCPCS directory has no drug-specific code for these products. Drugs dispensed by a pharmacy are billed by NDC. NDC vs J-code.
- Which NDC goes on a claim?
- The package NDC of what was given, in 11-digit form. How to convert a 10-digit NDC.