H.E.B BANANA

Product NDC
37808-919
11-digit product format
378080919
Labeler code
37808
Product ID
37808-919_2489f87a-061e-c0c7-e063-6394a90ad386
Type
HUMAN OTC DRUG
Nonproprietary name
SPF 50 Sunscreen
Dosage form
LOTION
Route
TOPICAL
Labeler
H.E.B
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-02-06
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 BANANA
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE45 mg/mL
OCTOCRYLENE80 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-919-12H.E.B BANANA237 mL in 1 TUBELOTION2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-919H.E.B BANANA (SPF 50 SUNSCREEN) LOTION [H.E.B]2Current NDC, Legacy NDC, 1 package rows20241017_b9a9837a-094b-4a57-a50c-5c1437deda7b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-919-1237808091912237 mL in 1 TUBE (37808-919-12) 237 ml2019-02-060000-00-00NoNoCurrent