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NDC 49967-736, Octinoxate, liquid, from L'Oreal USA Products Inc.

Product NDC
49967-736
Status
Listed
Labeler
L'Oreal USA Products Inc
Dosage form
LIQUID
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/49967-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OCTINOXATE30 mg/mL
Package NDCNDC-11Package
49967-736-01499670736011 TUBE in 1 CARTON (49967-736-01) / 32 mL in 1 TUBE

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 49967-736 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49967-736 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49967-736. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.