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NDC 49967-303, Octinoxate and Titanium dioxide, liquid, from L'Oreal USA Products Inc.
- Product NDC
- 49967-303
- 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
curl https://api.healthcare.dev/v1/drugs/ndc/49967-303 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OCTINOXATE67 mg/mL
- TITANIUM DIOXIDE115 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 49967-303-01 | 49967030301 | 1 BOTTLE in 1 CARTON (49967-303-01) / 30 mL in 1 BOTTLE |
| 49967-303-02 | 49967030302 | 100 mL in 1 TUBE (49967-303-02) |
| 49967-303-03 | 49967030303 | 1 mL in 1 PACKET (49967-303-03) |
| 49967-303-04 | 49967030304 | .4 mL in 1 PACKAGE (49967-303-04) |
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 49967-303 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/49967-303 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 49967-303. 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.