H.E.B

Product NDC
37808-975
11-digit product format
378080975
Labeler code
37808
Product ID
37808-975_c6b6d6b4-9346-5ea1-e053-2a95a90a70a9
Type
HUMAN OTC DRUG
Nonproprietary name
Ultra SPF 70 Continuous Spray
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
H.E.B
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-02-17
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
30; 150; 50; 100; 60 mg/g; 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
Brand name suffix
Solutions Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE150 mg/g
OCTISALATE50 mg/g
OCTOCRYLENE100 mg/g
OXYBENZONE60 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM, 95OOS7VE0Y

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-975-37H.E.BSolutions Sunscreen156 g in 1 CANAEROSOL, SPRAY1562

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-975H.E.B SOLUTIONS SUNSCREEN (ULTRA SPF 70 CONTINUOUS SPRAY) AEROSOL, SPRAY [H.E.B]2Current NDC, Legacy NDC, 1 package rows20241017_c16935ce-afdb-4571-b5a3-6dc5d01f721c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-975-3737808097537156 g in 1 CAN (37808-975-37) 156 g2012-02-170000-00-00NoNoCurrent