Skip to main content

Arizona Sun Sunscreen SPF15

NDC 61973-101 · Arizona Sun Products

FDA carries 4 listing records for this NDC; the most recent is shown.

Generic nameSunscreen
Dosage formLOTION
RouteTOPICAL
Active ingredient(s)OCTISALATE, OXYBENZONE, OCTINOXATE, AVOBENZONE
Strength20; 75; 30; 30 mg/g; mg/g; mg/g; mg/g
Marketing categoryOTC MONOGRAPH DRUG

Packages

61973-101-04 — 120 g in 1 BOTTLE (61973-101-04)

61973-101-08 — 946 g in 1 BOTTLE (61973-101-08)

61973-101-01 — 30 g in 1 BOTTLE (61973-101-01)

61973-101-03 — 90 g in 1 BOTTLE (61973-101-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

61957-3439 — OCTISALATE, TITANIUM DIOXIDE, 61957-3440 — OCTISALATE, TITANIUM DIOXIDE, 61957-3441 — OCTISALATE, TITANIUM DIOXIDE, 61957-3442 — OCTISALATE, TITANIUM DIOXIDE, 61957-3443 — OCTISALATE, TITANIUM DIOXIDE, 61957-3444 — OCTISALATE, TITANIUM DIOXIDE, 61957-3600 — AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 61957-3610 — ENSULIZOLE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, 61957-3620 — HOMOSALATE, OCTISALATE, OCTOCRYLENE, 61973-100 — Sunscreen, 61973-102 — Sunscreen, 61973-103 — Sunscreen, 61973-104 — Sunscreen, 61973-105 — Sunscreen, 61973-106 — Sunscreen, 61973-107 — Moisturizer, 61973-108 — Sunscreen, 61973-109 — Sunscreen, 61973-110 — Sunscreen, 61973-111 — Sunscreen, +4500 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.