H.E.B

Product NDC
37808-956
11-digit product format
378080956
Labeler code
37808
Product ID
37808-956_248a0777-7394-dea1-e063-6394a90a444a
Type
HUMAN OTC DRUG
Nonproprietary name
Ultra SPF 50 Lotion
Dosage form
LOTION
Route
TOPICAL
Labeler
H.E.B
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-02-20
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Active strength
20; 100; 50; 70; 60 mg/mL; 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
Brand name suffix
Solutions Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE20 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE70 mg/mL
OXYBENZONE60 mg/mL

Harmonized Identifiers#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-956-09H.E.BSolutions Sunscreen89 mL in 1 TUBELOTION892
37808-956-12H.E.BSolutions Sunscreen237 mL in 1 TUBELOTION2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-956H.E.B SOLUTIONS SUNSCREEN (ULTRA SPF 50 LOTION) LOTION [H.E.B]2Current NDC, Legacy NDC, 2 package rows20241017_12c76c72-4411-48d5-b79b-c58703bf1fdd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-956-093780809560989 mL in 1 TUBE (37808-956-09) 89 ml2012-02-200000-00-00NoNoCurrent
37808-956-1237808095612237 mL in 1 TUBE (37808-956-12) 237 ml2012-02-200000-00-00NoNoCurrent