NATURES CHOICE BABY- talc powder

Natures Choice Baby by

Drug Labeling and Warnings

Natures Choice Baby by is a Otc medication manufactured, distributed, or labeled by Unipack, Inc., Jell Pharmaceuticals Pvt. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Talc 99%

PURPOSE

Purpose

Skin Protectant

INDICATIONS & USAGE

Uses

It helps to absorb excess moisture, keeps the baby’s skin dry and soft for ultimate comfort.

WARNINGS

Warnings

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children.
• For external use only.
• Avoid contact with eyes, discontinue use if irritation persists.
• Avoid ingestion or accidental inhalation by baby. Seek professional assistance if needed.

DOSAGE & ADMINISTRATION

Directions

After changing diapers and after every bath dry baby’s skin thoroughly and apply liberally as needed.

INACTIVE INGREDIENT

Inactive Ingredient

Fragrance

PRINCIPAL DISPLAY PANEL

Package/Label Principal Display Panel

Natures Choice Baby Powder

Velvety Soft

NET WT 22 OZ (624 g)

INGREDIENTS AND APPEARANCE

NATURES CHOICE BABY 
talc powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43749-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TALC (UNII: 7SEV7J4R1U) (TALC - UNII:7SEV7J4R1U)	TALC	99 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43749-112-05	50 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
2	NDC: 43749-112-06	100 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
3	NDC: 43749-112-07	113 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
4	NDC: 43749-112-09	116 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
5	NDC: 43749-112-10	368 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
6	NDC: 43749-112-11	396 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
7	NDC: 43749-112-14	424 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016
8	NDC: 43749-112-15	624 g in 1 BOTTLE; Type 0: Not a Combination Product	06/07/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	06/07/2016

Labeler - Unipack, Inc. (009248480)

Registrant - Jell Pharmaceuticals Pvt. Ltd. (726025211)

Establishment
Name	Address	ID/FEI	Business Operations
Jell Pharmaceuticals Pvt. Ltd.		726025211	manufacture(43749-112)