KINLO ALWAYS GOLDEN BODY- zinc oxide lotion

KINLO ALWAYS GOLDEN BODY by

Drug Labeling and Warnings

KINLO ALWAYS GOLDEN BODY by is a Otc medication manufactured, distributed, or labeled by A-Frame SunCo Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ZINC OXIDE 10%

PURPOSE

SUNSCREEN

USES

• HELPS PREVENT SUNBURN
• IF USED AS DIRECTED WITH OTHER SUN PROTECTION MEASURES (SEE DIRECTIONS), DECREASES THE RISK OF SKIN CANCER AND EARLY SKIN AGING CAUSED BY THE SUN

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE ON BROKEN SKIN.

WHEN USING THIS PRODUCT KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

• APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE
• CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR
• USE A WATER-RESISTANT SUNSCREEN IF SWIMMING OR SWEATING
• REAPPLY AT LEAST EVERY 2 HOURS
• SUN PROTECTION MEASURES: SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY AGING. TO DECREASE THE RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUSING:
• LIMIT TIME IN THE SUN, ESPECIALLY FROM 10:00 A.M. TO 2 P.M.
• WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES
  

IMACTIVE INGREDIENTS

WATER, BUTYLENE GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, DIMETHICONE, CETEARYL ALCOHOL, CETEARYL OLIVATE, POLYGLYCERYL-3 DIISOSTEARATE, SORBITAN OLIVATE, CETEARYL GLUCOSIDE, ETHYLHEXYLGLYCERIN, PHENOXYETHANOL, TRIETHOXYCAPRYLYLSILANE, CAMELLIA SINENSIS (GREEN TEA) LEAF OIL, IRON OXIDES, TOCOPHERYL ACETATE, XANTHAN GUM, CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL.

OTHER INFORMATION

PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KINLO ALWAYS GOLDEN BODY 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82184-1001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
WATER (UNII: 059QF0KO0R)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
FERROUS OXIDE (UNII: G7036X8B5H)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)
SAFFLOWER OIL (UNII: 65UEH262IS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
JOJOBA OIL (UNII: 724GKU717M)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82184-1001-2	1 in 1 BOX	02/28/2022
1	NDC: 82184-1001-1	113 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 82184-1001-3	170 g in 1 TUBE; Type 0: Not a Combination Product	02/28/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/28/2022

Labeler - A-Frame SunCo Inc (118248026)