Bath and Body Works SPF
- Product NDC
- 62670-6864
- 11-digit product format
- 626706864
- Labeler code
- 62670
- Product ID
- 62670-6864_38d0d1d3-0655-99b6-e063-6394a90ac92d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone,Homosalate,Octisalate,Octocrylene
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bath & Body Works, Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-05
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3; 10; 5; 10 mg/100mg; mg/100mg; mg/100mg; mg/100mg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bath and Body Works SPF
- Brand name suffix
- Tahiti Isle
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTOCRYLENE | 3 mg/100mg |
| AVOBENZONE | 10 mg/100mg |
| HOMOSALATE | 5 mg/100mg |
| OCTISALATE | 10 mg/100mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5A68WGF6WM, G63QQF2NOX, V06SV4M95S, 4X49Y0596W |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62670-6864-0 | Bath and Body Works SPFTahiti Isle | 103 mg in 1 BOTTLE | GEL | 103 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62670-6864-0 | 62670686400 | 103 mg in 1 BOTTLE (62670-6864-0) | 103 mg | 2025-05-05 | No | No | Historical |