SNUGZ SPF 50 BROAD SPECTRUM SUNSCREEN- spf 50 broad spectrum sunscreen lotion

SnugZ SPF 50 Broad Spectrum Sunscreen by

Drug Labeling and Warnings

SnugZ SPF 50 Broad Spectrum Sunscreen by is a Otc medication manufactured, distributed, or labeled by SnugZ/USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

SPF 50 Broadspectrum Sunscreen Lotion

INGREDIENTS AND APPEARANCE

SNUGZ SPF 50 BROAD SPECTRUM SUNSCREEN 
spf 50 broad spectrum sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76309-551
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	4.5 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.7 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6.7 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
SUNFLOWER OIL (UNII: 3W1JG795YI)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
COCONUT OIL (UNII: Q9L0O73W7L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76309-551-01	28 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2019
2	NDC: 76309-551-19	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2019
3	NDC: 76309-551-02	56 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2019
4	NDC: 76309-551-04	112 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2019
5	NDC: 76309-551-08	226 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2019
6	NDC: 76309-551-51	30 mL in 1 TUBE; Type 0: Not a Combination Product	01/01/2019
7	NDC: 76309-551-61	39.75 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2019
8	NDC: 76309-551-62	85.17 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2019	12/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/01/2019

Labeler - SnugZ/USA, LLC (615959228)

Registrant - SnugZ/USA, LLC (615959228)

Establishment
Name	Address	ID/FEI	Business Operations
SnugZ/USA, LLC		615959228	manufacture(76309-551)