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SPF30 Sunscreen

NDC 70412-231 · Zhejiang Ayan Biotech Co., Ltd.

Generic nameAvobenzone, Homosalate, Octocrylene, Ocitsalate
Dosage formLOTION
RouteTOPICAL
Active ingredient(s)AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Strength30; 100; 50; 100 mg/mL; mg/mL; mg/mL; mg/mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

70412-231-15 15 mL in 1 BOTTLE (70412-231-15)

70412-231-20 20 mL in 1 BOTTLE (70412-231-20)

70412-231-30 30 mL in 1 BOTTLE (70412-231-30)

70412-231-35 35 mL in 1 BOTTLE (70412-231-35)

70412-231-45 45 mL in 1 BOTTLE (70412-231-45)

70412-231-53 53 mL in 1 BOTTLE (70412-231-53)

70412-231-60 60 mL in 1 BOTTLE (70412-231-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70325-3002 — OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE, 70325-3003 — OCTINOXATE, OCTOCRYLENE, OCTISALATE, and AVOBENZONE, 70381-125 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70381-130 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70381-131 — Avobenzone, Homosalate, Octisalate, and Octocrylene, 70381-132 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70381-133 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70392-020 — Octinoxate 7.50% Octisalate 5.00% Oxybenzone 4.00% Homosalate 10.00%, 70412-211 — AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, 70412-212 — AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, 70412-238 — Avobenzone, Homosalate, Octocrylene, Ocitsalate, 70412-316 — AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, 70453-001 — AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OXYBENZONE, 70541-128 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70541-210 — Avobenzone, Homosalate, Octisalate, Octrocrylene, 70541-211 — Avobenzone, Homosalate, Octisalate, Octocrylene, 70581-003 — AVOBENZONE, OCTISALATE, OCTOCRYLENE, 70581-020 — AVOBENZONE, OCTISALATE, OCTOCRYLENE, 70605-017 — Octinoxate and Octisalate, 70605-020 — AVOBENZONE, OCTINOXATE, OCTISALATE, and OCTOCRYLENE, +3818 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels