dr. brandt SUN SHIELD SPF 50
- Product NDC
- 81568-101
- 11-digit product format
- 815680101
- Labeler code
- 81568
- Product ID
- 81568-101_d6922659-fdc4-48c0-a7d6-a3051be051c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Dr. Brandt
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-02-15
- Substance
- ZINC OXIDE
- Active strength
- 17 g/100mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 81568-101_d6922659-fdc4-48c0-a7d6-a3051be051c1
- SPL ID
- d6922659-fdc4-48c0-a7d6-a3051be051c1
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- dr. brandt SUN SHIELD SPF 50
- Generic name
- Zinc Oxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Marketing start
- 2021-02-15
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M020
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ZINC OXIDE | 17 g/100mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | SOI2LOH54Z |
| Spl Set Id | 6f8af59b-d423-4250-8ddc-061fea886e3e |
| Manufacturer Name | Dr. Brandt |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 81568-101-50 | 1 BOTTLE, DROPPER in 1 BOX (81568-101-50) / 50 mL in 1 BOTTLE, DROPPER | 2021-02-15 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SOI2LOH54Z | ZINC OXIDE | 1314-13-2 | ZINC OXIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 81568-101-50 | 81568010150 | 1 BOTTLE, DROPPER in 1 BOX (81568-101-50) / 50 mL in 1 BOTTLE, DROPPER | 2021-02-15 | No | No | Historical |