NDC 37808-914 – H.e.b Ultra

Avobenzone 30 mg/mL; Homosalate 100 mg/mL; Octisalate 45 mg/mL; Octocrylene 80 mg/mL · Aerosol, Spray · Topical

Human Otc Drug

Product NDC37808-914

Product details

Brand name
H.e.b Ultra
Generic name
SPF 50 Sunscreen
Labeler
H.E.B
Dosage form
Aerosol, Spray
Route
Topical
Marketing category
OTC MONOGRAPH DRUG · M020
Marketed since
February 5, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for H.e.b Ultra →

Package NDC codes (1)

Package NDCDescriptionSince
37808-914-12237 mL in 1 TUBE (37808-914-12)Feb 5, 2019

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