FDA.reportPublic FDA data

HEB Solutions Sunscreen Face 50 Facial Mist Sunscreen

Product NDC
37808-127
11-digit product format
378080127
Labeler code
37808
Product ID
37808-127_0a387641-3b8a-38e0-e063-6294a90a81b3
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
SPRAY
Route
TOPICAL
Labeler
H.E.B
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-03-02
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 100; 50; 25 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
HEB Solutions Sunscreen Face 50 Facial Mist Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE100 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE25 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-127-04HEB Solutions Sunscreen Face 50 Facial Mist Sunscreen118 mL in 1 BOTTLE, SPRAYSPRAY1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-127HEB SOLUTIONS SUNSCREEN FACE 50 FACIAL MIST SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [H.E.B]2Current NDC, 1 package rows20231116_f6cdeb2f-fc58-1780-e053-6394a90a544a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37808-127-0437808012704118 mL in 1 BOTTLE, SPRAY (37808-127-04) 118 ml2020-03-02NoNoHistorical