SPF 50 FACIAL SUNSCREEN
- Product NDC
- 72860-000
- 11-digit product format
- 728600000
- Labeler code
- 72860
- Product ID
- 72860-000_98cd7ec4-650d-9250-e053-2a95a90aba9d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HOMOSALATE, OCTOCRYLENE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Beauty Architects, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-02-21
- Marketing end
- 2021-06-30
- Substance
- HOMOSALATE; OCTOCRYLENE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 70 mg/g; mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72860-000-13 | 72860000013 | 13 g in 1 CONTAINER (72860-000-13) | 13 g | 2019-02-21 | 2021-06-30 | No | No | Current |