NDC 37808-924

H.E.B ULTRA

Spf 30 Sunscreen

H.E.B ULTRA is a Topical Aerosol, Spray in the Human Otc Drug category. It is labeled and distributed by H.e.b. The primary component is Avobenzone; Homosalate; Octisalate; Octocrylene.

Product ID37808-924_703b49f8-e247-4391-8dd8-b5e9046d8ab8
NDC37808-924
Product TypeHuman Otc Drug
Proprietary NameH.E.B ULTRA
Generic NameSpf 30 Sunscreen
Dosage FormAerosol, Spray
Route of AdministrationTOPICAL
Marketing Start Date2019-04-24
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameH.E.B
Substance NameAVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active Ingredient Strength30 mg/g; mg/g; mg/g; mg/g
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 37808-924-37

156 g in 1 CAN (37808-924-37)
Marketing Start Date2019-04-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 37808-924-37 [37808092437]

H.E.B ULTRA AEROSOL, SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-24

Drug Details

Active Ingredients

IngredientStrength
AVOBENZONE30 mg/g

OpenFDA Data

SPL SET ID:90287874-cdfa-489c-936d-e487f6b3db96
Manufacturer
UNII
UPC Code
  • 0041220722037
  • NDC Crossover Matching brand name "H.E.B ULTRA" or generic name "Spf 30 Sunscreen"

    NDCBrand NameGeneric Name
    37808-914H.E.B ULTRASPF 50 Sunscreen
    37808-924H.E.B ULTRASPF 30 Sunscreen
    76150-244Big Cloud DefendSPF 30 Sunscreen

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.