NDC 37808-924 – H.e.b Ultra

Avobenzone 30 mg/g; Homosalate 100 mg/g; Octisalate 50 mg/g; Octocrylene 20 mg/g · Aerosol, Spray · Topical

Human Otc Drug

Product NDC37808-924

Product details

Brand name
H.e.b Ultra
Generic name
SPF 30 Sunscreen
Labeler
H.E.B
Dosage form
Aerosol, Spray
Route
Topical
Marketing category
OTC MONOGRAPH DRUG · M020
Marketed since
April 24, 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
37808-924-37156 g in 1 CAN (37808-924-37)Apr 24, 2019

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