H.E.B

Product NDC
37808-997
11-digit product format
378080997
Labeler code
37808
Product ID
37808-997_c71880ec-3660-4dcf-e053-2995a90a3485
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
2019-04-26
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 40 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
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE100 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE40 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-997-37H.E.B156 g in 1 CANAEROSOL, SPRAY1562

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-997H.E.B (SPF 50 SUNSCREEN) AEROSOL, SPRAY [H.E.B]2Current NDC, Legacy NDC, 1 package rows20241017_39bf1379-3dee-4aa0-967a-36faccca4216.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-997-3737808099737156 g in 1 CAN (37808-997-37) 156 g2019-04-260000-00-00NoNoCurrent