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Arizona Sun Sunscreen SPF 30

NDC 61973-102 · Arizona Sun Products

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

Generic nameSunscreen
Dosage formLOTION
RouteTOPICAL
Active ingredient(s)HOMOSALATE, OXYBENZONE, OCTINOXATE, AVOBENZONE, OCTISALATE
Strength30; 50; 75; 50; 30 mg/g; mg/g; mg/g; mg/g; mg/g
Marketing categoryOTC MONOGRAPH DRUG

Packages

61973-102-04 — .12 g in 1 BOTTLE (61973-102-04)

61973-102-01 — .03 g in 1 BOTTLE (61973-102-01)

61973-102-03 — .09 g in 1 BOTTLE (61973-102-03)

61973-102-08 — .946 g in 1 BOTTLE (61973-102-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 61973-101 — 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, 61973-112 — Sunscreen, +4602 more

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