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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
Request
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 NDCNDC-11Package
71889-350-08718890350081 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
curl https://api.healthcare.dev/v1/drugs/ndc/71889-350 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.