H.E.B ULTRA
- Product NDC
- 37808-924
- 11-digit product format
- 378080924
- Labeler code
- 37808
- Product ID
- 37808-924_c71836b9-92d1-6659-e053-2a95a90aa3a5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SPF 30 Sunscreen
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- H.E.B
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-04-24
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 50; 20 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- H.E.B ULTRA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 30 mg/g |
| HOMOSALATE | 100 mg/g |
| OCTISALATE | 50 mg/g |
| OCTOCRYLENE | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-924-37 | H.E.B ULTRA | 156 g in 1 CAN | AEROSOL, SPRAY | 156 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-924 | H.E.B ULTRA (SPF 30 SUNSCREEN) AEROSOL, SPRAY [H.E.B] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241017_90287874-cdfa-489c-936d-e487f6b3db96.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-924-37 | 37808092437 | 156 g in 1 CAN (37808-924-37) | 156 g | 2019-04-24 | 0000-00-00 | No | No | Current |