e.l.f. Camo CC Cream SPF 30 Fair 150 C

Product NDC
76354-182
11-digit product format
763540182
Labeler code
76354
Product ID
76354-182_407f9bf8-1163-b024-e063-6294a90a73ec
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
e.l.f. Cosmetics, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-09-18
Substance
HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
50; 45; 30; 63 mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
76354-182_407f9bf8-1163-b024-e063-6294a90a73ec
SPL ID
407f9bf8-1163-b024-e063-6294a90a73ec
Product type
HUMAN OTC DRUG
Finished product
Yes
Brand name base
e.l.f. Camo CC Cream SPF 30 Fair 150 C
Generic name
HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Marketing start
2025-09-18
Marketing category
OTC MONOGRAPH DRUG
Application number
M020
Listing expiration
2026-12-31

openFDA Active Ingredients

IngredientStrength
HOMOSALATE50 mg/g
OCTISALATE45 mg/g
OCTOCRYLENE30 mg/g
ZINC OXIDE63 mg/g

openFDA Harmonized Identifiers

FieldValues
Unii5A68WGF6WM, 4X49Y0596W, V06SV4M95S, SOI2LOH54Z
Spl Set Id407f9c0d-31c6-f5bb-e063-6394a90a4db4
Manufacturer Namee.l.f. Cosmetics, Inc.

openFDA Package Details

Package NDCDescriptionMarketing startSample
76354-182-011 TUBE in 1 CARTON (76354-182-01) / 30 g in 1 TUBE2025-09-19No

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V06SV4M95SHOMOSALATE118-56-9HOMOSALATE
4X49Y0596WOCTISALATE118-60-5OCTISALATE
5A68WGF6WMOCTOCRYLENE6197-30-4OCTOCRYLENE
SOI2LOH54ZZINC OXIDE1314-13-2ZINC OXIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76354-182-01763540182011 TUBE in 1 CARTON (76354-182-01) / 30 g in 1 TUBE1 tube2025-09-19NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Camo CC Cream SPF 30e.l.f. Cosmetics, Inc.2025-09-18HUMAN OTC DRUG LABEL1