Jergens Natural Glow
- Product NDC
- 10596-720
- 11-digit product format
- 105960720
- Labeler code
- 10596
- Product ID
- 10596-720_5c53d20f-c294-915c-e063-6294a90a7d36
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Kao USA Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-21
- Substance
- OCTISALATE; HOMOSALATE; AVOBENZONE; OCTOCRYLENE
- Active strength
- 50; 70; 30; 50 mg/mL; mg/mL; mg/mL; mg/mL
- 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
- Jergens Natural Glow
- Brand name suffix
- Medium to Deep
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OCTISALATE | 50 mg/mL |
| HOMOSALATE | 70 mg/mL |
| AVOBENZONE | 30 mg/mL |
| OCTOCRYLENE | 50 mg/mL |
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 |
|---|---|---|---|---|---|---|---|
| 10596-720-30 | 10596072030 | 88 mL in 1 TUBE (10596-720-30) | 88 ml | 2026-09-21 | No | No | Current |