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Obagi-C C-Rx System Normal-Dry Skin Intervention

NDC 62032-922, HYDROQUINONE, TITANIUM DIOXIDE, ZINC OXIDE, kit, from Obagi Cosmeceuticals LLC.

Product NDC
62032-922
Status
Listed
Labeler
Obagi Cosmeceuticals LLC
Dosage form
KIT
Route
—
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62032-922 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
62032-922-01620320922011 KIT in 1 BAG (62032-922-01) * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 177 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-105-36) * 1 BOTTLE, GLASS in 1 CARTON (62032-106-10) / 30 mL in 1 BOTTLE, GLASS

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 62032-922 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62032-922 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62032-922. 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.