FDA.reportPublic FDA data

Every. Single. Face. Watery SPF 50

Product NDC
75936-652
11-digit product format
759360652
Labeler code
75936
Product ID
75936-652_47fcc6e6-af01-b5dc-e063-6294a90ac671
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Supergoop, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-11-11
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 9; 5; 9 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Every. Single. Face. Watery SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE9 g/100mL
OCTISALATE5 g/100mL
OCTOCRYLENE9 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75936-652-01Every. Single. Face. Watery SPF 501.5 mL in 1 PACKETLOTION1.55
75936-652-02Every. Single. Face. Watery SPF 5010 mL in 1 TUBELOTION105
75936-652-03Every. Single. Face. Watery SPF 5050 mL in 1 BOTTLELOTION505

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
75936-652-01759360652011.5 mL in 1 PACKET (75936-652-01) 1.5 ml2022-01-15NoNoHistorical
75936-652-027593606520210 mL in 1 TUBE (75936-652-02) 10 ml2022-01-15NoNoHistorical
75936-652-037593606520350 mL in 1 BOTTLE (75936-652-03) 50 ml2021-11-11NoNoHistorical