NDC 37808-914

H.E.B ULTRA

Spf 50 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 ID: 37808-914_f8370b01-75d9-49cc-b644-95458541f721
• NDC: 37808-914
• Product Type: Human Otc Drug
• Proprietary Name: H.E.B ULTRA
• Generic Name: Spf 50 Sunscreen
• Dosage Form: Aerosol, Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-02-05
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: H.E.B
• Substance Name: AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
• Active Ingredient Strength: 30 mg/mL; mg/mL; mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 37808-914-12

237 mL in 1 TUBE (37808-914-12)

• Marketing Start Date: 2019-02-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 37808-914-12 [37808091412]

H.E.B ULTRA AEROSOL, SPRAY

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-02-05

Drug Details

Active Ingredients

Ingredient	Strength
AVOBENZONE	30 mg/mL

OpenFDA Data

• SPL SET ID: d6184ba2-0e47-459a-8777-1f27be2140a6
• Manufacturer:
  • H.E.B
• UNII:
  • G63QQF2NOX
  • 4X49Y0596W
  • 5A68WGF6WM
  • V06SV4M95S
• UPC Code:
  • 0041220721702

NDC Crossover Matching brand name "H.E.B ULTRA" or generic name "Spf 50 Sunscreen"

NDC	Brand Name	Generic Name
37808-914	H.E.B ULTRA	SPF 50 Sunscreen
37808-924	H.E.B ULTRA	SPF 30 Sunscreen
37808-910	H.E.B	SPF 50 Sunscreen
37808-912	H.E.B	SPF 50 Sunscreen
37808-996	H.E.B	SPF 50 Sunscreen
37808-997	H.E.B	SPF 50 Sunscreen
37808-998	H.E.B	SPF 50 Sunscreen
37808-913	H.E.B BABY	SPF 50 Sunscreen
37808-919	H.E.B BANANA	SPF 50 Sunscreen
37808-916	H.E.B MANGO	SPF 50 Sunscreen
37808-918	H.E.B MANGO	SPF 50 Sunscreen