Kids Mineral Sunscreen SPF 50
- Product NDC
- 73418-111
- 11-digit product format
- 734180111
- Labeler code
- 73418
- Product ID
- 73418-111_5b19f2bc-0df5-c427-e063-6394a90a0a45
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Hello Bello
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-09
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 22.25; 4.82 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kids Mineral Sunscreen SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC OXIDE | 22.25 mg/g |
| TITANIUM DIOXIDE | 4.82 mg/g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 73418-111-01 | 73418011101 | 142 g in 1 BOTTLE, SPRAY (73418-111-01) | 142 g | 2026-09-09 | No | No | Current |