H.E.B ULTRA
- Product NDC
- 37808-914
- 11-digit product format
- 378080914
- Labeler code
- 37808
- Product ID
- 37808-914_c6b84cf6-4361-5352-e053-2995a90a2717
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SPF 50 Sunscreen
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- H.E.B
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-05
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30; 100; 45; 80 mg/mL; mg/mL; mg/mL; mg/mL
- 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/mL |
| HOMOSALATE | 100 mg/mL |
| OCTISALATE | 45 mg/mL |
| OCTOCRYLENE | 80 mg/mL |
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 |
|---|
| 37808-914-12 | H.E.B ULTRA | 237 mL in 1 TUBE | AEROSOL, SPRAY | 237 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-914 | H.E.B ULTRA (SPF 50 SUNSCREEN) AEROSOL, SPRAY [H.E.B] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241017_d6184ba2-0e47-459a-8777-1f27be2140a6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-914-12 | 37808091412 | 237 mL in 1 TUBE (37808-914-12) | 237 ml | 2019-02-05 | 0000-00-00 | No | No | Current |